4-75174280-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174280
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174280
    reference: chr 4
allele count: 1
allele frequency: 8.260912665631299e-6
allele num: 121052
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.30T>C
  hgvsp: ENST00000503098.1:c.30T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.30T>C
  hgvsp: ENST00000332112.4:c.30T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.30T>C
  hgvsp: ENST00000413830.1:c.30T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.30T>C
  hgvsp: ENST00000505212.1:c.30T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.30T>C
  hgvsp: ENST00000502358.1:c.30T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.30T>C
  hgvsp: ENST00000509145.1:c.30T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.30T>C
  hgvsp: ENST00000502835.1:c.30T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.30T>C
  hgvsp: ENST00000514968.1:c.30T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4122
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr10Tyr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-75174292-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174292
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174292
    reference: chr 4
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.42C>A
  hgvsp: ENSP00000425890.1:p.Asn14Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.42C>A
  hgvsp: ENSP00000330375.4:p.Asn14Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.42C>A
  hgvsp: ENSP00000423090.1:p.Asn14Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.42C>A
  hgvsp: ENSP00000426630.1:p.Asn14Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.42C>A
  hgvsp: ENSP00000411898.1:p.Asn14Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.42C>A
  hgvsp: ENSP00000426678.1:p.Asn14Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.42C>A
  hgvsp: ENSP00000424392.1:p.Asn14Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.42C>A
  hgvsp: ENSP00000426550.1:p.Asn14Lys
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4712
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6852
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asn14Lys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

4-75174292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174292
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174292
    reference: chr 4
allele count: 19
allele frequency: 1.569962486159541e-4
allele num: 121022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.42C>T
  hgvsp: ENST00000509145.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.42C>T
  hgvsp: ENST00000332112.4:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.42C>T
  hgvsp: ENST00000514968.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.42C>T
  hgvsp: ENST00000502835.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.42C>T
  hgvsp: ENST00000413830.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.42C>T
  hgvsp: ENST00000503098.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.42C>T
  hgvsp: ENST00000505212.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.42C>T
  hgvsp: ENST00000502358.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2802
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
hgvs: c.42C>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-75174293-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174293
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174293
    reference: chr 4
allele count: 2
allele frequency: 1.65264671371201e-5
allele num: 121018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.43G>A
  hgvsp: ENSP00000423090.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.43G>A
  hgvsp: ENSP00000411898.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43G>A
  hgvsp: ENSP00000426630.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.43G>A
  hgvsp: ENSP00000330375.4:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.43G>A
  hgvsp: ENSP00000425890.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.43G>A
  hgvsp: ENSP00000426678.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.43G>A
  hgvsp: ENSP00000424392.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.43G>A
  hgvsp: ENSP00000426550.1:p.Ala15Thr
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12275
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala15Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

4-75174300-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174300
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174300
    reference: chr 4
allele count: 5
allele frequency: 4.133256179217988e-5
allele num: 120970
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.43+7A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.43+7A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.43+7A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+7A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.43+7A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.43+7A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.43+7A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.43+7A>G
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12257
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3263
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4118
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2801
  bin: 7.25e1
  variant carriers: 0
hgvs: c.43+7A>G
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

4-75174306-CTTTTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174306
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174301
    reference: chr 4
allele count: 4
allele frequency: 3.309231100153879e-5
allele num: 120874
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.43+21_43+25delTTGTT
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.43+21_43+25delTTGTT
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+21_43+25delTTGTT
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.43+21_43+25delTTGTT
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.43+21_43+25delTTGTT
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.43+21_43+25delTTGTT
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.43+21_43+25delTTGTT
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.43+21_43+25delTTGTT
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8194
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4703
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: CTTTTG
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

4-75174310-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174310
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174310
    reference: chr 4
allele count: 1
allele frequency: 8.27787159365584e-6
allele num: 120804
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.43+17T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.43+17T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.43+17T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+17T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.43+17T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.43+17T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.43+17T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.43+17T>G
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13763
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4699
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4114
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

4-75174312-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174312
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174312
    reference: chr 4
allele count: 1
allele frequency: 8.283219853221344e-6
allele num: 120726
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.43+19T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.43+19T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.43+19T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+19T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.43+19T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.43+19T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.43+19T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.43+19T>C
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2767
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4112
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

4-75174325-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174325
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174325
    reference: chr 4
allele count: 34
allele frequency: 2.820125744430252e-4
allele num: 120562
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.43+32A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.43+32A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.43+32A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.43+32A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.43+32A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+32A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.43+32A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.43+32A>G
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8128
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12646
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11791
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6250
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4636
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

4-75174328-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174328
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174328
    reference: chr 4
allele count: 366
allele frequency: 3.03578241900433e-3
allele num: 120562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+35T>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.43+35T>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.43+35T>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.43+35T>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.43+35T>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.43+35T>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.43+35T>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.43+35T>A
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 11651
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 8119
  bin: 3.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 5.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 4.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 4.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12397
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 9.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 5.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 4079
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6166
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 7
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-75174329-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174329
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174328
    reference: chr 4
allele count: 3
allele frequency: 2.489461280578883e-5
allele num: 120508
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.43+37delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.43+37delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.43+37delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+37delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.43+37delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.43+37delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.43+37delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.43+37delA
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6143
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2676
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4088
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: CA
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

4-75174335-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174335
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174335
    reference: chr 4
allele count: 1
allele frequency: 8.310617645103384e-6
allele num: 120328
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.43+42A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.43+42A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+42A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.43+42A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.43+42A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.43+42A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.43+42A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.43+42A>G
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10766
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4554
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1645
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1926
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1936
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-75174344-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174344
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174344
    reference: chr 4
allele count: 1
allele frequency: 8.339866228545694e-6
allele num: 119906
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.43+51A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.43+51A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.43+51A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.43+51A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.43+51A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.43+51A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.43+51A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+51A>G
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4488
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6618
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1779
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

4-75174760-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174760
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174760
    reference: chr 4
allele count: 2
allele frequency: 1.649294102124291e-5
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-50T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-50T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-50T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+467T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-50T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-50T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-50T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-50T>C
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9262
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6960
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2749
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2426
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1263
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/4-75174761-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174761
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174761
    reference: chr 4
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-49A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-49A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-49A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-49A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-49A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+468A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-49A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-49A>C
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6958
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

4-75174763-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174763
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174763
    reference: chr 4
allele count: 2
allele frequency: 1.649212501030758e-5
allele num: 121270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-47A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+470A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-47A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-47A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-47A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-47A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-47A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-47A>G
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

4-75174764-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174764
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174764
    reference: chr 4
allele count: 10
allele frequency: 8.246198502490352e-5
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+471T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-46T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-46T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-46T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-46T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-46T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-46T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-46T>C
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9253
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

4-75174766-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174766
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174765
    reference: chr 4
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-42delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+475delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-42delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-42delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-42delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-42delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-42delA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-42delA
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9261
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6936
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2747
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: GA
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

4-75174772-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174772
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174772
    reference: chr 4
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-38G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-38G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+479G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-38G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-38G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-38G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-38G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-38G>A
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 15939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9260
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2738
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

4-75174774-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174774
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174774
    reference: chr 4
allele count: 3
allele frequency: 2.473737157181259e-5
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-36C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-36C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-36C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-36C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+481C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-36C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-36C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-36C>T
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33238
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2734
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9245
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

4-75174776-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174776
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174776
    reference: chr 4
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-34C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-34C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-34C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-34C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-34C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-34C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+483C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-34C>T
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2402
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3511
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2739
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

4-75174786-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174786
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174786
    reference: chr 4
allele count: 8
allele frequency: 6.594566077552098e-5
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-24G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+493G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-24G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-24G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-24G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-24G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-24G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-24G>T
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9267
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

4-75174789-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174789
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174789
    reference: chr 4
allele count: 882
allele frequency: 7.270509100501187e-3
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-21G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-21G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+496G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-21G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-21G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-21G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-21G>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-21G>T
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 4.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 24620
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 15933
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 3.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 5.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 9.75e1
  variant carriers: 662
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 33450
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9257
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3497
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 10
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

4-75174798-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174798
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174798
    reference: chr 4
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-12C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-12C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+505C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-12C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-12C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-12C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-12C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-12C>G
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9406
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2768
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

4-75174802-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174802
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174802
    reference: chr 4
allele count: 2
allele frequency: 1.648478454386601e-5
allele num: 121324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-8T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+509T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-8T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-8T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-8T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-8T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-8T>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-8T>G
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: c.44-8T>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum

4-75174803-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174803
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174803
    reference: chr 4
allele count: 2
allele frequency: 1.648478454386601e-5
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+510A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-7A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-7A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-7A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-7A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-7A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-7A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-7A>T
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6230
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2771
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
hgvs: c.44-7A>T
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

4-75174804-ATAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174804
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174801
    reference: chr 4
allele count: 2
allele frequency: 1.648451280022419e-5
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+512_43+514delTAC
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-5_44-3delTAC
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-5_44-3delTAC
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-5_44-3delTAC
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-5_44-3delTAC
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-5_44-3delTAC
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-5_44-3delTAC
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-5_44-3delTAC
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34007
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9410
  bin: 6.75e1
  variant carriers: 0
hgvs: c.44-5_44-3delTAC
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: ATAC
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

4-75174805-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174805
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174805
    reference: chr 4
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-5T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-5T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+512T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-5T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-5T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-5T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-5T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-5T>C
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2769
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: c.44-5T>C
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ

4-75174806-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174806
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174806
    reference: chr 4
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-4A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-4A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-4A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-4A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-4A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-4A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-4A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+513A>T
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9409
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33995
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: c.44-4A>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

4-75174809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174809
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174809
    reference: chr 4
allele count: 4
allele frequency: 3.296739524610161e-5
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.44-1G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.44-1G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.44-1G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.44-1G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.44-1G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+516G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.44-1G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.44-1G>A
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6225
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 9410
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: c.44-1G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-75174815-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174815
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174814
    reference: chr 4
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.50delC
  hgvsp: ENSP00000423090.1:p.Thr17LysfsTer3
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.50delC
  hgvsp: ENSP00000426550.1:p.Thr17LysfsTer3
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.50delC
  hgvsp: ENSP00000330375.4:p.Thr17LysfsTer3
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.50delC
  hgvsp: ENSP00000411898.1:p.Thr17LysfsTer3
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.3delC
  hgvsp: ENSP00000398415.2:p.Thr2LysfsTer3
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.50delC
  hgvsp: ENSP00000426678.1:p.Thr17LysfsTer3
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.50delC
  hgvsp: ENSP00000424392.1:p.Thr17LysfsTer3
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.50delC
  hgvsp: ENSP00000425890.1:p.Thr17LysfsTer3
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+523delC
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34039
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr17LysfsTer3
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: AC
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

4-75174818-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174818
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174818
    reference: chr 4
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.52G>A
  hgvsp: ENSP00000426550.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.52G>A
  hgvsp: ENSP00000423090.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.52G>A
  hgvsp: ENSP00000330375.4:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.52G>A
  hgvsp: ENSP00000425890.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.52G>A
  hgvsp: ENSP00000411898.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.52G>A
  hgvsp: ENSP00000426678.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.52G>A
  hgvsp: ENSP00000424392.1:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+525G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.5G>A
  hgvsp: ENSP00000398415.2:p.Ala3Thr
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3537
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala18Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

4-75174826-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174826
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174826
    reference: chr 4
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.13C>G
  hgvsp: ENST00000446430.2:c.13C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.60C>G
  hgvsp: ENST00000502835.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.60C>G
  hgvsp: ENST00000505212.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.60C>G
  hgvsp: ENST00000332112.4:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.60C>G
  hgvsp: ENST00000514968.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.60C>G
  hgvsp: ENST00000502358.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.60C>G
  hgvsp: ENST00000413830.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.60C>G
  hgvsp: ENST00000503098.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+533C>G
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2412
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34055
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr20Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

4-75174826-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174826
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174826
    reference: chr 4
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.60C>T
  hgvsp: ENST00000514968.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.60C>T
  hgvsp: ENST00000502358.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.13C>T
  hgvsp: ENST00000446430.2:c.13C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.60C>T
  hgvsp: ENST00000505212.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.60C>T
  hgvsp: ENST00000503098.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.60C>T
  hgvsp: ENST00000332112.4:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.60C>T
  hgvsp: ENST00000502835.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.60C>T
  hgvsp: ENST00000413830.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+533C>T
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9405
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2412
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr20Thr
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: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

4-75174827-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174827
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174827
    reference: chr 4
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.61G>A
  hgvsp: ENSP00000426550.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.61G>A
  hgvsp: ENSP00000330375.4:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.61G>A
  hgvsp: ENSP00000424392.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+534G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.61G>A
  hgvsp: ENSP00000426678.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.61G>A
  hgvsp: ENSP00000423090.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.61G>A
  hgvsp: ENSP00000425890.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.14G>A
  hgvsp: ENSP00000398415.2:p.Glu6Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.61G>A
  hgvsp: ENSP00000411898.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2768
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu21Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

4-75174830-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174830
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174830
    reference: chr 4
allele count: 2
allele frequency: 1.648098094798602e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.64G>A
  hgvsp: ENSP00000425890.1:p.Glu22Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.64G>A
  hgvsp: ENSP00000426550.1:p.Glu22Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.64G>A
  hgvsp: ENSP00000423090.1:p.Glu22Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.64G>A
  hgvsp: ENSP00000330375.4:p.Glu22Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.17G>A
  hgvsp: ENSP00000398415.2:p.Glu7Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.64G>A
  hgvsp: ENSP00000424392.1:p.Glu22Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.64G>A
  hgvsp: ENSP00000411898.1:p.Glu22Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.64G>A
  hgvsp: ENSP00000426678.1:p.Glu22Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+537G>A
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 954
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu22Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

4-75174838-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174838
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174838
    reference: chr 4
allele count: 404
allele frequency: 3.329158151493177e-3
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.72C>T
  hgvsp: ENST00000505212.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.25C>T
  hgvsp: ENST00000446430.2:c.25C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.72C>T
  hgvsp: ENST00000502358.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.72C>T
  hgvsp: ENST00000502835.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.72C>T
  hgvsp: ENST00000503098.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.72C>T
  hgvsp: ENST00000332112.4:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.72C>T
  hgvsp: ENST00000514968.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.72C>T
  hgvsp: ENST00000413830.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+545C>T
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 25030
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16130
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 9.75e1
  variant carriers: 290
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3515
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala24Ala
num of homozygotes: 2
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

4-75174839-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174839
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174839
    reference: chr 4
allele count: 5
allele frequency: 4.120245236996506e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.73G>A
  hgvsp: ENSP00000425890.1:p.Val25Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.73G>A
  hgvsp: ENSP00000411898.1:p.Val25Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.73G>A
  hgvsp: ENSP00000330375.4:p.Val25Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.73G>A
  hgvsp: ENSP00000423090.1:p.Val25Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.73G>A
  hgvsp: ENSP00000424392.1:p.Val25Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.26G>A
  hgvsp: ENSP00000398415.2:p.Val10Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+546G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.73G>A
  hgvsp: ENSP00000426550.1:p.Val25Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.73G>A
  hgvsp: ENSP00000426678.1:p.Val25Met
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25202
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16234
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6954
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val25Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

4-75174846-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174846
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174846
    reference: chr 4
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.80T>C
  hgvsp: ENSP00000423090.1:p.Val27Ala
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.80T>C
  hgvsp: ENSP00000330375.4:p.Val27Ala
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.80T>C
  hgvsp: ENSP00000426550.1:p.Val27Ala
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.80T>C
  hgvsp: ENSP00000424392.1:p.Val27Ala
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.80T>C
  hgvsp: ENSP00000425890.1:p.Val27Ala
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.80T>C
  hgvsp: ENSP00000411898.1:p.Val27Ala
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.80T>C
  hgvsp: ENSP00000426678.1:p.Val27Ala
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+553T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.33T>C
  hgvsp: ENSP00000398415.2:p.Val12Ala
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9457
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3532
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val27Ala
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

4-75174853-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174853
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174853
    reference: chr 4
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.40T>A
  hgvsp: ENST00000446430.2:c.40T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.87T>A
  hgvsp: ENST00000514968.1:c.87T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.87T>A
  hgvsp: ENST00000502835.1:c.87T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.87T>A
  hgvsp: ENST00000502358.1:c.87T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.87T>A
  hgvsp: ENST00000503098.1:c.87T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.87T>A
  hgvsp: ENST00000505212.1:c.87T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+560T>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.87T>A
  hgvsp: ENST00000413830.1:c.87T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.87T>A
  hgvsp: ENST00000332112.4:c.87T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34302
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro29Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

4-75174857-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174857
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174857
    reference: chr 4
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.91A>G
  hgvsp: ENSP00000423090.1:p.Ile31Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.91A>G
  hgvsp: ENSP00000425890.1:p.Ile31Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.91A>G
  hgvsp: ENSP00000426550.1:p.Ile31Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.91A>G
  hgvsp: ENSP00000426678.1:p.Ile31Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.91A>G
  hgvsp: ENSP00000411898.1:p.Ile31Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.44A>G
  hgvsp: ENSP00000398415.2:p.Ile16Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.91A>G
  hgvsp: ENSP00000424392.1:p.Ile31Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+564A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.91A>G
  hgvsp: ENSP00000330375.4:p.Ile31Val
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2775
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile31Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

4-75174859-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174859
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174859
    reference: chr 4
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.93C>T
  hgvsp: ENST00000505212.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.93C>T
  hgvsp: ENST00000514968.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.93C>T
  hgvsp: ENST00000502358.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.93C>T
  hgvsp: ENST00000502835.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.46C>T
  hgvsp: ENST00000446430.2:c.46C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+566C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.93C>T
  hgvsp: ENST00000413830.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.93C>T
  hgvsp: ENST00000332112.4:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.93C>T
  hgvsp: ENST00000503098.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34281
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile31Ile
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-75174860-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174860
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174860
    reference: chr 4
allele count: 2
allele frequency: 1.648559982854976e-5
allele num: 121318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.94A>C
  hgvsp: ENSP00000425890.1:p.Thr32Pro
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.47A>C
  hgvsp: ENSP00000398415.2:p.Thr17Pro
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.94A>C
  hgvsp: ENSP00000330375.4:p.Thr32Pro
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.94A>C
  hgvsp: ENSP00000423090.1:p.Thr32Pro
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+567A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.94A>C
  hgvsp: ENSP00000411898.1:p.Thr32Pro
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.94A>C
  hgvsp: ENSP00000426678.1:p.Thr32Pro
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.94A>C
  hgvsp: ENSP00000426550.1:p.Thr32Pro
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.94A>C
  hgvsp: ENSP00000424392.1:p.Thr32Pro
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr32Pro
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

4-75174863-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174863
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174863
    reference: chr 4
allele count: 2
allele frequency: 1.648723063986942e-5
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.97G>A
  hgvsp: ENSP00000425890.1:p.Ala33Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.97G>A
  hgvsp: ENSP00000426550.1:p.Ala33Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.97G>A
  hgvsp: ENSP00000411898.1:p.Ala33Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.97G>A
  hgvsp: ENSP00000423090.1:p.Ala33Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.97G>A
  hgvsp: ENSP00000426678.1:p.Ala33Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.97G>A
  hgvsp: ENSP00000424392.1:p.Ala33Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.97G>A
  hgvsp: ENSP00000330375.4:p.Ala33Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.50G>A
  hgvsp: ENSP00000398415.2:p.Ala18Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+570G>A
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala33Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum

http://identifiers.org/exac.variant/4-75174866-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174866
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174866
    reference: chr 4
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+573C>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.100C>A
  hgvsp: ENSP00000426550.1:p.Gln34Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.100C>A
  hgvsp: ENSP00000424392.1:p.Gln34Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.100C>A
  hgvsp: ENSP00000423090.1:p.Gln34Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.53C>A
  hgvsp: ENSP00000398415.2:p.Gln19Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.100C>A
  hgvsp: ENSP00000425890.1:p.Gln34Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.100C>A
  hgvsp: ENSP00000426678.1:p.Gln34Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.100C>A
  hgvsp: ENSP00000411898.1:p.Gln34Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.100C>A
  hgvsp: ENSP00000330375.4:p.Gln34Lys
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln34Lys
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

4-75174882-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174882
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174882
    reference: chr 4
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.59+10C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.106+10C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.116C>G
  hgvsp: ENSP00000426678.1:p.Thr39Arg
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.116C>G
  hgvsp: ENSP00000425890.1:p.Thr39Arg
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.116C>G
  hgvsp: ENSP00000411898.1:p.Thr39Arg
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+589C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.106+10C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.106+10C>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.116C>G
  hgvsp: ENSP00000423090.1:p.Thr39Arg
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr39Arg
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-75174884-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174884
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174884
    reference: chr 4
allele count: 5
allele frequency: 4.125684863687372e-5
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.106+12G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.106+12G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+591G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.59+12G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.118G>A
  hgvsp: ENSP00000411898.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.118G>A
  hgvsp: ENSP00000426678.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.118G>A
  hgvsp: ENSP00000423090.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.118G>A
  hgvsp: ENSP00000425890.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.106+12G>A
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1260
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val40Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

4-75174887-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174887
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174887
    reference: chr 4
allele count: 1
allele frequency: 8.25559316436886e-6
allele num: 121130
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.59+15A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.106+15A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.121A>T
  hgvsp: ENSP00000426678.1:p.Asn41Tyr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.106+15A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+594A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.121A>T
  hgvsp: ENSP00000425890.1:p.Asn41Tyr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.121A>T
  hgvsp: ENSP00000411898.1:p.Asn41Tyr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.121A>T
  hgvsp: ENSP00000423090.1:p.Asn41Tyr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.106+15A>T
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9386
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn41Tyr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

4-75174890-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174890
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174890
    reference: chr 4
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.106+18A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+597A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.124A>G
  hgvsp: ENSP00000423090.1:p.Lys42Glu
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.106+18A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.124A>G
  hgvsp: ENSP00000426678.1:p.Lys42Glu
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.124A>G
  hgvsp: ENSP00000425890.1:p.Lys42Glu
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.106+18A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.59+18A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.124A>G
  hgvsp: ENSP00000411898.1:p.Lys42Glu
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys42Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

4-75174896-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174896
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174896
    reference: chr 4
allele count: 1
allele frequency: 8.263779852904718e-6
allele num: 121010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.59+24G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.106+24G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.130G>A
  hgvsp: ENSP00000423090.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.130G>A
  hgvsp: ENSP00000426678.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.130G>A
  hgvsp: ENSP00000425890.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.106+24G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+603G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.106+24G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.130G>A
  hgvsp: ENSP00000411898.1:p.Glu44Lys
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3506
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu44Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

4-75174899-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174899
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174899
    reference: chr 4
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.133G>A
  hgvsp: ENSP00000426678.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.106+27G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.133G>A
  hgvsp: ENSP00000425890.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.106+27G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.133G>A
  hgvsp: ENSP00000411898.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.106+27G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.59+27G>A
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.133G>A
  hgvsp: ENSP00000423090.1:p.Ala45Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+606G>A
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3495
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala45Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

4-75174901-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174901
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174901
    reference: chr 4
allele count: 1
allele frequency: 8.27348843366317e-6
allele num: 120868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+608T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.106+29T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.106+29T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.59+29T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.133+2T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.133+2T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.106+29T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.133+2T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.133+2T>C
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: c.133+2T>C
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

4-75174909-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174909
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174909
    reference: chr 4
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.133+10T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+616T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.133+10T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.133+10T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.133+10T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.106+37T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.106+37T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.59+37T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.106+37T>C
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33189
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

4-75174911-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174911
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174911
    reference: chr 4
allele count: 89
allele frequency: 7.401124305624854e-4
allele num: 120252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.133+12C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.133+12C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.106+39C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.133+12C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.133+12C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.106+39C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+618C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.106+39C>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.59+39C>T
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15477
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24690
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 5.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5871
  bin: 9.75e1
  variant carriers: 88
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2342
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

4-75174917-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174917
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174917
    reference: chr 4
allele count: 1
allele frequency: 8.35952651641811e-6
allele num: 119624
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.133+18T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.106+45T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.106+45T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.59+45T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.106+45T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+624T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.133+18T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.133+18T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.133+18T>C
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2580
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31619
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

4-75174919-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75174919
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75174919
    reference: chr 4
allele count: 1
allele frequency: 8.38321345338095e-6
allele num: 119286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.43+626A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.133+20A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.133+20A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.133+20A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.133+20A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.59+47A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.106+47A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.106+47A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.106+47A>G
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2863
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/4-75177856-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177856
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177856
    reference: chr 4
allele count: 1
allele frequency: 8.476300264460568e-6
allele num: 117976
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.134-46A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.60-46A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.107-46A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.134-46A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.44-46A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.134-46A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.134-46A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.107-46A>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.107-46A>C
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4909
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2496
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

4-75177862-GAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177862
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177860
    reference: chr 4
allele count: 1
allele frequency: 8.468978133098461e-6
allele num: 118078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.60-36_60-35delCA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.134-36_134-35delCA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.107-36_107-35delCA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.44-36_44-35delCA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.107-36_107-35delCA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.107-36_107-35delCA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.134-36_134-35delCA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.134-36_134-35delCA
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.134-36_134-35delCA
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: GAC
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

4-75177872-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177872
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177872
    reference: chr 4
allele count: 3
allele frequency: 2.532756990409294e-5
allele num: 118448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.107-30A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.107-30A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.134-30A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.134-30A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.44-30A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.134-30A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.60-30A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.134-30A>G
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.107-30A>G
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

4-75177880-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177880
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177880
    reference: chr 4
allele count: 1
allele frequency: 8.417366710998132e-6
allele num: 118802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.107-22A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.134-22A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.134-22A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.134-22A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.107-22A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.107-22A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.134-22A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.44-22A>T
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.60-22A>T
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

4-75177896-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177896
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177896
    reference: chr 4
allele count: 1
allele frequency: 8.342370901810295e-6
allele num: 119870
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.134-6T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.107-6T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.134-6T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.134-6T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.134-6T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.44-6T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.60-6T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.107-6T>C
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.107-6T>C
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 7.25e1
  variant carriers: 0
hgvs: c.134-6T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS

4-75177902-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177902
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177902
    reference: chr 4
allele count: 1
allele frequency: 8.319744417451495e-6
allele num: 120196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.107C>T
  hgvsp: ENSP00000424392.1:p.Ala36Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.134C>T
  hgvsp: ENSP00000423090.1:p.Ala45Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.134C>T
  hgvsp: ENSP00000425890.1:p.Ala45Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.134C>T
  hgvsp: ENSP00000426678.1:p.Ala45Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.107C>T
  hgvsp: ENSP00000330375.4:p.Ala36Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.60C>T
  hgvsp: ENSP00000398415.2:p.Ala21Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.107C>T
  hgvsp: ENSP00000426550.1:p.Ala36Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.44C>T
  hgvsp: ENSP00000426630.1:p.Ala15Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.134C>T
  hgvsp: ENSP00000411898.1:p.Ala45Val
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala45Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

4-75177908-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177908
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177908
    reference: chr 4
allele count: 1
allele frequency: 8.292836647703714e-6
allele num: 120586
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.113A>G
  hgvsp: ENSP00000426550.1:p.Asn38Ser
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.140A>G
  hgvsp: ENSP00000426678.1:p.Asn47Ser
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.140A>G
  hgvsp: ENSP00000423090.1:p.Asn47Ser
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.113A>G
  hgvsp: ENSP00000330375.4:p.Asn38Ser
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.66A>G
  hgvsp: ENSP00000398415.2:p.Asn23Ser
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.50A>G
  hgvsp: ENSP00000426630.1:p.Asn17Ser
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.140A>G
  hgvsp: ENSP00000411898.1:p.Asn47Ser
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.113A>G
  hgvsp: ENSP00000424392.1:p.Asn38Ser
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.140A>G
  hgvsp: ENSP00000425890.1:p.Asn47Ser
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn47Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

4-75177911-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177911
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177911
    reference: chr 4
allele count: 15
allele frequency: 1.242050874403815e-4
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.143T>C
  hgvsp: ENSP00000425890.1:p.Ile48Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.143T>C
  hgvsp: ENSP00000423090.1:p.Ile48Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.143T>C
  hgvsp: ENSP00000426678.1:p.Ile48Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.53T>C
  hgvsp: ENSP00000426630.1:p.Ile18Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.116T>C
  hgvsp: ENSP00000424392.1:p.Ile39Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.116T>C
  hgvsp: ENSP00000330375.4:p.Ile39Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.143T>C
  hgvsp: ENSP00000411898.1:p.Ile48Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.116T>C
  hgvsp: ENSP00000426550.1:p.Ile39Thr
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.69T>C
  hgvsp: ENSP00000398415.2:p.Ile24Thr
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4945
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 1474
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile48Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

4-75177912-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177912
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177912
    reference: chr 4
allele count: 1
allele frequency: 8.278693953241936e-6
allele num: 120792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.70A>G
  hgvsp: ENSP00000398415.2:p.Ile24Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.144A>G
  hgvsp: ENSP00000426678.1:p.Ile48Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.144A>G
  hgvsp: ENSP00000411898.1:p.Ile48Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.117A>G
  hgvsp: ENSP00000330375.4:p.Ile39Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.117A>G
  hgvsp: ENSP00000426550.1:p.Ile39Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.144A>G
  hgvsp: ENSP00000423090.1:p.Ile48Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.54A>G
  hgvsp: ENSP00000426630.1:p.Ile18Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.144A>G
  hgvsp: ENSP00000425890.1:p.Ile48Met
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.117A>G
  hgvsp: ENSP00000424392.1:p.Ile39Met
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5092
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile48Met
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

4-75177917-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177917
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177917
    reference: chr 4
allele count: 17
allele frequency: 1.405376806322542e-4
allele num: 120964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.122G>A
  hgvsp: ENSP00000330375.4:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.59G>A
  hgvsp: ENSP00000426630.1:p.Gly20Glu
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.122G>A
  hgvsp: ENSP00000424392.1:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.149G>A
  hgvsp: ENSP00000425890.1:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.75G>A
  hgvsp: ENSP00000398415.2:p.Gly26Glu
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.122G>A
  hgvsp: ENSP00000426550.1:p.Gly41Glu
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.149G>A
  hgvsp: ENSP00000423090.1:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.149G>A
  hgvsp: ENSP00000411898.1:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.149G>A
  hgvsp: ENSP00000426678.1:p.Gly50Glu
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4939
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1711
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly50Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

4-75177918-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177918
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177918
    reference: chr 4
allele count: 3
allele frequency: 2.479666732791113e-5
allele num: 120984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.60A>G
  hgvsp: ENST00000509145.1:c.60A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.123A>G
  hgvsp: ENST00000332112.4:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.150A>G
  hgvsp: ENST00000413830.1:c.150A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.123A>G
  hgvsp: ENST00000514968.1:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.150A>G
  hgvsp: ENST00000502835.1:c.150A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.150A>G
  hgvsp: ENST00000502358.1:c.150A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.123A>G
  hgvsp: ENST00000505212.1:c.123A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.150A>G
  hgvsp: ENST00000503098.1:c.150A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.76A>G
  hgvsp: ENST00000446430.2:c.76A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5092
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4918
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly50Gly
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

4-75177922-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177922
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177922
    reference: chr 4
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.154A>G
  hgvsp: ENSP00000425890.1:p.Ile52Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.154A>G
  hgvsp: ENSP00000423090.1:p.Ile52Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.127A>G
  hgvsp: ENSP00000330375.4:p.Ile43Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.154A>G
  hgvsp: ENSP00000426678.1:p.Ile52Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.64A>G
  hgvsp: ENSP00000426630.1:p.Ile22Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.127A>G
  hgvsp: ENSP00000426550.1:p.Ile43Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.80A>G
  hgvsp: ENSP00000398415.2:p.Ile28Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.154A>G
  hgvsp: ENSP00000411898.1:p.Ile52Val
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.127A>G
  hgvsp: ENSP00000424392.1:p.Ile43Val
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile52Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/4-75177940-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177940
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177940
    reference: chr 4
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.145C>A
  hgvsp: ENSP00000330375.4:p.His49Asn
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.82C>A
  hgvsp: ENSP00000426630.1:p.His28Asn
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.172C>A
  hgvsp: ENSP00000411898.1:p.His58Asn
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.172C>A
  hgvsp: ENSP00000426678.1:p.His58Asn
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.145C>A
  hgvsp: ENSP00000426550.1:p.His49Asn
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.172C>A
  hgvsp: ENSP00000425890.1:p.His58Asn
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.145C>A
  hgvsp: ENSP00000424392.1:p.His49Asn
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.172C>A
  hgvsp: ENSP00000423090.1:p.His58Asn
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.98C>A
  hgvsp: ENSP00000398415.2:p.His34Asn
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 9.25e1
  variant carriers: 0
hgvs: p.His58Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/4-75177943-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 75177943
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 75177943
    reference: chr 4
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000411898
  ensembl transcript: ENST00000413830
  gene symbol: EPGN
  hgvsc: ENST00000413830.1:c.175C>A
  hgvsp: ENSP00000411898.1:p.Leu59Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426630
  ensembl transcript: ENST00000509145
  gene symbol: EPGN
  hgvsc: ENST00000509145.1:c.85C>A
  hgvsp: ENSP00000426630.1:p.Leu29Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426550
  ensembl transcript: ENST00000514968
  gene symbol: EPGN
  hgvsc: ENST00000514968.1:c.148C>A
  hgvsp: ENSP00000426550.1:p.Leu50Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000425890
  ensembl transcript: ENST00000503098
  gene symbol: EPGN
  hgvsc: ENST00000503098.1:c.175C>A
  hgvsp: ENSP00000425890.1:p.Leu59Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000398415
  ensembl transcript: ENST00000446430
  gene symbol: EPGN
  hgvsc: ENST00000446430.2:c.101C>A
  hgvsp: ENSP00000398415.2:p.Leu35Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000423090
  ensembl transcript: ENST00000502835
  gene symbol: EPGN
  hgvsc: ENST00000502835.1:c.175C>A
  hgvsp: ENSP00000423090.1:p.Leu59Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000426678
  ensembl transcript: ENST00000502358
  gene symbol: EPGN
  hgvsc: ENST00000502358.1:c.175C>A
  hgvsp: ENSP00000426678.1:p.Leu59Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000424392
  ensembl transcript: ENST00000505212
  gene symbol: EPGN
  hgvsc: ENST00000505212.1:c.148C>A
  hgvsp: ENSP00000424392.1:p.Leu50Ile
  variant of: http://identifiers.org/hgnc/17470
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182585
  ensembl protein: ENSP00000330375
  ensembl transcript: ENST00000332112
  gene symbol: EPGN
  hgvsc: ENST00000332112.4:c.148C>A
  hgvsp: ENSP00000330375.4:p.Leu50Ile
  variant of: http://identifiers.org/hgnc/17470
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu59Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C

GenotypeQuality
all individuals: 19407
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3263
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6858
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4715
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17276
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.143e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

DP
type: SiteQuality
SIO_000300: 2.617011e6

VQSLOD
type: SiteQuality
SIO_000300: -7.09e-1

QD
type: SiteQuality
SIO_000300: 9.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.025e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 6.234e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19305
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3262
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2802
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1948
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4118
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17282
bin: 9.75e1
variant carriers: 1

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.85e-1

DP
type: SiteQuality
SIO_000300: 2.616387e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.264e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
all individuals: 19305
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4712
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 246
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6852
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3262
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4118
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17282
bin: 9.75e1
variant carriers: 19

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

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.251981743934662e-4
allele num: 66608
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.738223535546671e-4
allele num: 11506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169317118802619e-4
allele num: 8552
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

QD
type: SiteQuality
SIO_000300: 1.264e1

DP
type: SiteQuality
SIO_000300: 2.616387e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

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

GenotypeQuality
all individuals: 1948
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6849
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4120
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2801
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4712
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3263
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19285
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17269
bin: 9.75e1
variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.075334143377886e-5
allele num: 16460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 2.487e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.615267e6

QD
type: SiteQuality
SIO_000300: 1.062e1

VQSLOD
type: SiteQuality
SIO_000300: 9.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

GenotypeQuality
all individuals: 6840
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 331
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4707
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17267
bin: 9.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 19174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 5
allele frequency: 5.847953216374269e-4
allele num: 8550
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-2

FS
type: SiteQuality
SIO_000300: 2.242e0

MQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

QD
type: SiteQuality
SIO_000300: 1.33e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 2.613545e6

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6800
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18877
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17265
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4114
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.341372044017794e-4
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.934e0

FS
type: SiteQuality
SIO_000300: 5.511e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

MQ
type: SiteQuality
SIO_000300: 5.231e1

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

DP
type: SiteQuality
SIO_000300: 2.609952e6

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

GenotypeQuality
all individuals: 102
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17262
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18637
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6758
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2784
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e0

QD
type: SiteQuality
SIO_000300: 1.491e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.073e0

DP
type: SiteQuality
SIO_000300: 2.606229e6

FS
type: SiteQuality
SIO_000300: 4.091e0

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504030802550836e-5
allele num: 66488
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.42e-1

QD
type: SiteQuality
SIO_000300: 1.187e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

DP
type: SiteQuality
SIO_000300: 2.600613e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 34

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4091
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 5.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 20
allele frequency: 2.347417840375587e-3
allele num: 8520
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.892960462873674e-4
allele num: 10370
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.227144434899988e-4
allele num: 16298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.355135965308519e-4
allele num: 66414
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.541e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.64e0

DP
type: SiteQuality
SIO_000300: 2.574256e6

GenotypeQuality
all individuals: 1208
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 358

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2684
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variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 17
allele frequency: 1.480062685007836e-3
allele num: 11486
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.066732090284593e-4
allele num: 16304
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.023914942321014e-5
allele num: 66402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

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

African
type: Population
allele count: 340
allele frequency: 3.277424330055909e-2
allele num: 10374
num of homozygotes: 7

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.11e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.48e0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.461e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

FS
type: SiteQuality
SIO_000300: 9.86e-1

DP
type: SiteQuality
SIO_000300: 2.568997e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.613e0

GenotypeQuality
all individuals: 217
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15205
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variant carriers: 0

GenotypeQuality
all individuals: 3250
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variant carriers: 0

GenotypeQuality
all individuals: 455
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variant carriers: 0

GenotypeQuality
all individuals: 4618
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 147
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 1938
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GenotypeQuality
all individuals: 17142
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variant carriers: 3

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.519297399897563e-5
allele num: 66382
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.543e1

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.021e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.559743e6

GenotypeQuality
all individuals: 709
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3241
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
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variant carriers: 0

GenotypeQuality
all individuals: 1376
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
all individuals: 571
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 5599
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variant carriers: 0

GenotypeQuality
all individuals: 17132
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variant carriers: 1

GenotypeQuality
all individuals: 12564
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variant carriers: 0

GenotypeQuality
all individuals: 4066
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variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.658103148541626e-5
allele num: 10354
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16222
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66320
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.817e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

FS
type: SiteQuality
SIO_000300: 1.967e0

QD
type: SiteQuality
SIO_000300: 1.131e1

VQSLOD
type: SiteQuality
SIO_000300: -1.954e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

DP
type: SiteQuality
SIO_000300: 2.529613e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.012e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

GenotypeQuality
all individuals: 3268
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variant carriers: 0

GenotypeQuality
all individuals: 41
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GenotypeQuality
all individuals: 1931
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variant carriers: 0

GenotypeQuality
all individuals: 2341
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3499
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variant carriers: 0

GenotypeQuality
all individuals: 3237
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512584704743466e-5
allele num: 66112
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

FS
type: SiteQuality
SIO_000300: 1.1401e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.921e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.76e0

DP
type: SiteQuality
SIO_000300: 2.503002e6

VQSLOD
type: SiteQuality
SIO_000300: -1.413e0

MQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.85e-1

QD
type: SiteQuality
SIO_000300: 1.467e1

GenotypeQuality
all individuals: 65
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 73
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 143
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variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3548
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999850007499625e-5
allele num: 66670
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 6.146e0

VQSLOD
type: SiteQuality
SIO_000300: 6.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.08e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

DP
type: SiteQuality
SIO_000300: 2.143079e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.65e-1

QD
type: SiteQuality
SIO_000300: 1.435e1

GenotypeQuality
all individuals: 2745
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
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variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32849
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variant carriers: 0

GenotypeQuality
all individuals: 9255
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variant carriers: 0

GenotypeQuality
all individuals: 2427
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variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.25e1
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GenotypeQuality
all individuals: 3548
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 141
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.846e0

VQSLOD
type: SiteQuality
SIO_000300: -1.038e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.17e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

QD
type: SiteQuality
SIO_000300: 1.531e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.69e0

DP
type: SiteQuality
SIO_000300: 2.142816e6

GenotypeQuality
all individuals: 954
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9249
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32990
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 6948
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2741
bin: 7.25e1
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GenotypeQuality
all individuals: 3526
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variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.39e-2

FS
type: SiteQuality
SIO_000300: 2.423e0

QD
type: SiteQuality
SIO_000300: 9.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 2.142892e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.202e0

MQRankSum
type: SiteQuality
SIO_000300: 3.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.223e0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33027
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6946
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2743
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3518
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 9
allele frequency: 8.655510675129833e-4
allele num: 10398
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

QD
type: SiteQuality
SIO_000300: 1.44e1

FS
type: SiteQuality
SIO_000300: 1.632e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

VQSLOD
type: SiteQuality
SIO_000300: 4.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

DP
type: SiteQuality
SIO_000300: 2.142846e6

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

GenotypeQuality
all individuals: 3519
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33083
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2406
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1265
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.16e-1

MQ
type: SiteQuality
SIO_000300: 5.992e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.64e-2

DP
type: SiteQuality
SIO_000300: 2.14228e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.86e-1

FS
type: SiteQuality
SIO_000300: 7.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e0

QD
type: SiteQuality
SIO_000300: 1.376e1

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

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

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3526
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33229
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6932
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.45e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.19e-1

QD
type: SiteQuality
SIO_000300: 7.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

VQSLOD
type: SiteQuality
SIO_000300: -3.105e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.033e0

DP
type: SiteQuality
SIO_000300: 2.142873e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.741e0

GenotypeQuality
all individuals: 6929
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3516
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1263
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2403
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.316423442205235e-4
allele num: 8634
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.871e0

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 2.143274e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.095e0

QD
type: SiteQuality
SIO_000300: 1.183e1

FS
type: SiteQuality
SIO_000300: 2.068e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.21e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

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

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9258
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33326
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6926
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

MQRankSum
type: SiteQuality
SIO_000300: 4.34e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.247e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.696e0

QD
type: SiteQuality
SIO_000300: 1.282e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.24e-1

DP
type: SiteQuality
SIO_000300: 2.142973e6

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

GenotypeQuality
all individuals: 2402
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33453
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3511
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6926
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

African
type: Population
allele count: 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: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.199364336901442e-4
allele num: 66702
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.93e-1

QD
type: SiteQuality
SIO_000300: 1.208e1

DP
type: SiteQuality
SIO_000300: 2.144222e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.439e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2730
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7020
bin: 9.75e1
variant carriers: 872

GenotypeQuality
all individuals: 2386
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 9.25e1
variant carriers: 1

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

African
type: Population
allele count: 10
allele frequency: 9.613535858488752e-4
allele num: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.315886984715146e-4
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 715
allele frequency: 1.071899736147757e-2
allele num: 66704
num of homozygotes: 8

Latino
type: Population
allele count: 75
allele frequency: 6.494631104953239e-3
allele num: 11548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.537205081669691e-4
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 11
allele frequency: 1.211453744493392e-2
allele num: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 66
allele frequency: 3.999515210277542e-3
allele num: 16502
num of homozygotes: 2

FS
type: SiteQuality
SIO_000300: 5.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.052e0

QD
type: SiteQuality
SIO_000300: 1.253e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.27e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.33e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 2.175069e6

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

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3542
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33987
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6232
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 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: 11550
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.676e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.783e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 5.867e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.84e-2

FS
type: SiteQuality
SIO_000300: 1.997e0

DP
type: SiteQuality
SIO_000300: 2.076606e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.477e0

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

QD
type: SiteQuality
SIO_000300: 9.08e0

GenotypeQuality
all individuals: 40
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2769
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1265
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34002
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3542
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9407
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6230
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998141152485459e-5
allele num: 66708
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.69e-2

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
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MQ
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SIO_000300: 5.977e1

DP
type: SiteQuality
SIO_000300: 2.076811e6

FS
type: SiteQuality
SIO_000300: 4.435e0

BaseQRankSum
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SIO_000300: 5.58e0

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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bin: 8.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.99805126667666e-5
allele num: 66710
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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ReadPosRankSum
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QD
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MQRankSum
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DP
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FS
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.977e1

BaseQRankSum
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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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bin: 7.25e1
variant carriers: 0

Latino
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allele frequency: 1.731301939058172e-4
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66710
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

QD
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DP
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FS
type: SiteQuality
SIO_000300: 1.0209e1

MQRankSum
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SIO_000300: 9.22e-1

ClippingRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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SIO_000300: 2.92e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.916e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-2

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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DP
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SIO_000300: 2.076172e6

FS
type: SiteQuality
SIO_000300: 5.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.131e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.137e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.68e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.24e-2

QD
type: SiteQuality
SIO_000300: 1.79e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 5.995743022454058e-5
allele num: 66714
num of homozygotes: 0

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

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

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

South Asian
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VQSLOD
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MQ
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QD
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BaseQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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Other
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European (Non-Finnish)
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allele num: 66722
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South Asian
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VQSLOD
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MQRankSum
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DP
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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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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

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

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

Latino
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num of homozygotes: 0

East Asian
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allele frequency: 1.158480074142725e-4
allele num: 8632
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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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num of homozygotes: 0

Other
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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MQ
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BaseQRankSum
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DP
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-1

DP
type: SiteQuality
SIO_000300: 2.075956e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 5.237e0

QD
type: SiteQuality
SIO_000300: 1.09e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.884e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

MQRankSum
type: SiteQuality
SIO_000300: -4.3e-2

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997242536866083e-5
allele num: 66728
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.503e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.244e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 1.018e1

VQSLOD
type: SiteQuality
SIO_000300: 2.05e-1

DP
type: SiteQuality
SIO_000300: 2.075606e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997152704930316e-5
allele num: 66730
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e0

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

FS
type: SiteQuality
SIO_000300: 1.153e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.197e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.159999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.075425e6

MQ
type: SiteQuality
SIO_000300: 5.988e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 402

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
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 1256
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 318
allele frequency: 4.765472800839203e-3
allele num: 66730
num of homozygotes: 1

African
type: Population
allele count: 7
allele frequency: 6.728181468665898e-4
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.058681185722928e-3
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.038781163434903e-3
allele num: 11552
num of homozygotes: 0

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

South Asian
type: Population
allele count: 59
allele frequency: 3.573591762568141e-3
allele num: 16510
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 1.104e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 1.895e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.75e-1

DP
type: SiteQuality
SIO_000300: 2.087466e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 2778
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 5898
bin: 9.75e1
variant carriers: 5

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.49288176232579e-5
allele num: 66730
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.88e0

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.317e0

DP
type: SiteQuality
SIO_000300: 2.045144e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.941e1

QD
type: SiteQuality
SIO_000300: 1.155e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.833e0

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

GenotypeQuality
all individuals: 40
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.044224e6

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

FS
type: SiteQuality
SIO_000300: 7.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.23e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

QD
type: SiteQuality
SIO_000300: 1.489e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.97e-1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.043864e6

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

GenotypeQuality
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variant carriers: 0

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

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

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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QD
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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
all individuals: 12
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GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 5889
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 8.534000000000001e0

QD
type: SiteQuality
SIO_000300: 6.61e0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

MQRankSum
type: SiteQuality
SIO_000300: -2.21e-1

DP
type: SiteQuality
SIO_000300: 2.043438e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.027e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.67e0

QD
type: SiteQuality
SIO_000300: 1.317e1

FS
type: SiteQuality
SIO_000300: 2.902e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 2.043345e6

VQSLOD
type: SiteQuality
SIO_000300: 6.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3519
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.207e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.75e-1

DP
type: SiteQuality
SIO_000300: 2.043104e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.954e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 4.951e0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

GenotypeQuality
all individuals: 65
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 3520
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.654e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.361e0

MQRankSum
type: SiteQuality
SIO_000300: -1.173e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.46e-1

QD
type: SiteQuality
SIO_000300: 2.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.271e0

DP
type: SiteQuality
SIO_000300: 2.042696e6

GenotypeQuality
all individuals: 1259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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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
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5880
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 4.074e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.44e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.711e0

QD
type: SiteQuality
SIO_000300: 1.071e1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 2.040514e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.293e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

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: 949
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.423654871546292e-4
allele num: 16504
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: 1
allele frequency: 1.16333178222429e-4
allele num: 8596
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.28e-1

QD
type: SiteQuality
SIO_000300: 1.268e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.85e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
type: SiteQuality
SIO_000300: 9.28e-1

FS
type: SiteQuality
SIO_000300: 2.491e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.895e0

DP
type: SiteQuality
SIO_000300: 2.039992e6

MQRankSum
type: SiteQuality
SIO_000300: -2.32e-1

GenotypeQuality
all individuals: 5875
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 17
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.396e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.2e0

DP
type: SiteQuality
SIO_000300: 2.037823e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.434e0

VQSLOD
type: SiteQuality
SIO_000300: -1.306e-1

QD
type: SiteQuality
SIO_000300: 1.276e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.165229550221394e-4
allele num: 8582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.93e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.53e0

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.903e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.47e-1

QD
type: SiteQuality
SIO_000300: 1.602e1

GenotypeQuality
all individuals: 947
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 331
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 2745
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.739e0

DP
type: SiteQuality
SIO_000300: 2.033996e6

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 1.34e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.261e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33872
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.168224299065421e-4
allele num: 8560
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.699e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.64e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

DP
type: SiteQuality
SIO_000300: 2.031813e6

VQSLOD
type: SiteQuality
SIO_000300: -1.289e0

GenotypeQuality
all individuals: 3493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2735
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503895088278642e-5
allele num: 66494
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.029403e6

QD
type: SiteQuality
SIO_000300: 1.57e1

FS
type: SiteQuality
SIO_000300: 3.178e0

MQRankSum
type: SiteQuality
SIO_000300: -1.323e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.969e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.06e-1

MQ
type: SiteQuality
SIO_000300: 5.827e1

GenotypeQuality
all individuals: 218
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9054
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.084205402774397e-5
allele num: 16436
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

FS
type: SiteQuality
SIO_000300: 5.845e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 2.00982e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

QD
type: SiteQuality
SIO_000300: 1.551e1

VQSLOD
type: SiteQuality
SIO_000300: 4.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 27
bin: 2.5e0
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1236
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.622836160167862e-4
allele num: 11438
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

African
type: Population
allele count: 86
allele frequency: 8.325266214908035e-3
allele num: 10330
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

QD
type: SiteQuality
SIO_000300: 1.418e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.565e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

DP
type: SiteQuality
SIO_000300: 2.001207e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8489
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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: 129
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.752291788570315e-5
allele num: 10254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65786
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
SIO_000300: -8.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

QD
type: SiteQuality
SIO_000300: 1.485e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.957382e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2536
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5765
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.119951040391677e-5
allele num: 16340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65592
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.85e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

QD
type: SiteQuality
SIO_000300: 1.166e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.932479e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519941634241245e-5
allele num: 65792
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.879e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.14e0

QD
type: SiteQuality
SIO_000300: 1.638e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

DP
type: SiteQuality
SIO_000300: 3.550252e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 286
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variant carriers: 0

GenotypeQuality
all individuals: 1707
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.976419701409237e-5
allele num: 14334
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.14e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.554834e6

QD
type: SiteQuality
SIO_000300: 1.712e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 4.92e0

GenotypeQuality
all individuals: 1423
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 1708
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GenotypeQuality
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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: 825
bin: 3.25e1
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GenotypeQuality
all individuals: 1280
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65914
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 2.05987366108212e-4
allele num: 14564
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.742e0

QD
type: SiteQuality
SIO_000300: 1.141e1

DP
type: SiteQuality
SIO_000300: 3.562993e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 2.677e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14776
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.208e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.334e0

DP
type: SiteQuality
SIO_000300: 3.572201e6

FS
type: SiteQuality
SIO_000300: 1.154e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e0

VQSLOD
type: SiteQuality
SIO_000300: -1.192e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

QD
type: SiteQuality
SIO_000300: 9.84e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

VQSLOD
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.65e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-3

QD
type: SiteQuality
SIO_000300: 1.392e1

DP
type: SiteQuality
SIO_000300: 3.589848e6

FS
type: SiteQuality
SIO_000300: 1.934e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.354855109303508e-5
allele num: 15736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66376
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.924e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.361e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.49e-2

FS
type: SiteQuality
SIO_000300: 6.879999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.26e0

VQSLOD
type: SiteQuality
SIO_000300: -1.123e0

DP
type: SiteQuality
SIO_000300: 3.596862e6

QD
type: SiteQuality
SIO_000300: 1.193e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.863e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 52
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GenotypeQuality
all individuals: 1385
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
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: 1
allele frequency: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15992
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 1.589e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.57e0

VQSLOD
type: SiteQuality
SIO_000300: 4.42e-1

QD
type: SiteQuality
SIO_000300: 1.4e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.601847e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 15

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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.10450363778486e-4
allele num: 66524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16130
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

DP
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QD
type: SiteQuality
SIO_000300: 1.335e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.659999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.195019204559534e-5
allele num: 16142
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 2.59e0

VQSLOD
type: SiteQuality
SIO_000300: -2.512e-1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.66e-1

QD
type: SiteQuality
SIO_000300: 1.532e1

GenotypeQuality
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variant carriers: 0

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

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

Other
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South Asian
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allele count: 17
allele frequency: 1.045639069996309e-3
allele num: 16258
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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QD
type: SiteQuality
SIO_000300: 1.197e1

MQ
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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DP
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: -2.955e0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.505180958101817e-5
allele num: 66590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

QD
type: SiteQuality
SIO_000300: 1.186e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.607536e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.18e-1

MQ
type: SiteQuality
SIO_000300: 5.921e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e-1

GenotypeQuality
all individuals: 1380
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1323
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45761
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6977
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1521
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.982e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.113e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.379e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.44e-1

DP
type: SiteQuality
SIO_000300: 3.609256e6

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7190
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1316
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45761
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.847e0

FS
type: SiteQuality
SIO_000300: 4.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 3.611713e6

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

QD
type: SiteQuality
SIO_000300: 1.334e1

GenotypeQuality
all individuals: 87
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 878
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1315
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1380
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45761
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 738
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7208
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
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: 8624
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0