4-15009950-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15009950
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15009950
    reference: chr 4
allele count: 8
allele frequency: 6.637131431795178e-5
allele num: 120534
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+740A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1756T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.634-12A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+740A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+731A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+740A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.1945-12A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1756T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+731A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.1945-12A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.634-12A>G
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25133
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20974
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5882
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

4-15009968-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15009968
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15009968
    reference: chr 4
allele count: 1
allele frequency: 8.269520202437855e-6
allele num: 120926
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+758T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.1951T>C
  hgvsp: ENSP00000443985.1:p.Ser651Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.640T>C
  hgvsp: ENSP00000259997.5:p.Ser214Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.1951T>C
  hgvsp: ENSP00000437884.1:p.Ser651Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+758T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1774A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+749T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+749T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+758T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.640T>C
  hgvsp: ENSP00000424084.1:p.Ser214Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1774A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser651Pro
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

4-15009981-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15009981
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15009981
    reference: chr 4
allele count: 1
allele frequency: 8.262004692818665e-6
allele num: 121036
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+762T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1787A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+771T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.653T>C
  hgvsp: ENSP00000259997.5:p.Leu218Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.653T>C
  hgvsp: ENSP00000424084.1:p.Leu218Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1787A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+771T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.1964T>C
  hgvsp: ENSP00000437884.1:p.Leu655Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.1964T>C
  hgvsp: ENSP00000443985.1:p.Leu655Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+762T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+771T>C
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu655Ser
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

4-15009986-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15009986
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15009986
    reference: chr 4
allele count: 5
allele frequency: 4.129228329809725e-5
allele num: 121088
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+776G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.1969G>C
  hgvsp: ENSP00000437884.1:p.Ala657Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1792C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1792C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.658G>C
  hgvsp: ENSP00000259997.5:p.Ala220Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+776G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+767G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.1969G>C
  hgvsp: ENSP00000443985.1:p.Ala657Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.658G>C
  hgvsp: ENSP00000424084.1:p.Ala220Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+767G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+776G>C
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala657Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

4-15009993-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15009993
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15009993
    reference: chr 4
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1799C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+774G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.665G>T
  hgvsp: ENSP00000424084.1:p.Gly222Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+783G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1799C>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.1976G>T
  hgvsp: ENSP00000443985.1:p.Gly659Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.1976G>T
  hgvsp: ENSP00000437884.1:p.Gly659Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+783G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.665G>T
  hgvsp: ENSP00000259997.5:p.Gly222Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+774G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+783G>T
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1339
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly659Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

4-15010004-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010004
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010004
    reference: chr 4
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+785C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+785C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.1987C>G
  hgvsp: ENSP00000437884.1:p.Leu663Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1810G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1810G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+794C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.676C>G
  hgvsp: ENSP00000259997.5:p.Leu226Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.1987C>G
  hgvsp: ENSP00000443985.1:p.Leu663Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.676C>G
  hgvsp: ENSP00000424084.1:p.Leu226Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+794C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+794C>G
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu663Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-15010009-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010009
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010009
    reference: chr 4
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+790A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.681A>G
  hgvsp: ENST00000507071.1:c.681A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+799A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+799A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+790A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.681A>G
  hgvsp: ENST00000259997.5:c.681A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1815T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.1992A>G
  hgvsp: ENST00000541112.1:c.1992A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+799A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.1992A>G
  hgvsp: ENST00000538197.1:c.1992A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1815T>C
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln664Gln
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

4-15010012-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010012
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010012
    reference: chr 4
allele count: 4
allele frequency: 3.30338266384778e-5
allele num: 121088
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.1995T>C
  hgvsp: ENST00000541112.1:c.1995T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+793T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1818A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+793T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.1995T>C
  hgvsp: ENST00000538197.1:c.1995T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.684T>C
  hgvsp: ENST00000507071.1:c.684T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+802T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1818A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.684T>C
  hgvsp: ENST00000259997.5:c.684T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+802T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+802T>C
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7759
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp665Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

4-15010029-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010029
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010029
    reference: chr 4
allele count: 1
allele frequency: 8.289674381590291e-6
allele num: 120632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+810C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.701C>T
  hgvsp: ENSP00000259997.5:p.Ala234Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.701C>T
  hgvsp: ENSP00000424084.1:p.Ala234Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2012C>T
  hgvsp: ENSP00000443985.1:p.Ala671Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1835G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2012C>T
  hgvsp: ENSP00000437884.1:p.Ala671Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+819C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+810C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+819C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1835G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+819C>T
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala671Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

4-15010035-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010035
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010035
    reference: chr 4
allele count: 1
allele frequency: 8.300408380092301e-6
allele num: 120476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1841G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2018C>T
  hgvsp: ENSP00000437884.1:p.Thr673Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.707C>T
  hgvsp: ENSP00000424084.1:p.Thr236Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1841G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+816C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2018C>T
  hgvsp: ENSP00000443985.1:p.Thr673Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+825C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+825C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+816C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.707C>T
  hgvsp: ENSP00000259997.5:p.Thr236Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+825C>T
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5935
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr673Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

4-15010064-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010064
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010064
    reference: chr 4
allele count: 9
allele frequency: 7.786544850498338e-5
allele num: 115584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+845G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+854G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+854G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+854G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2034+13G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.723+13G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.723+13G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2034+13G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1870C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1870C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+845G>A
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20103
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7495
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17534
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7451
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

4-15010066-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010066
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010066
    reference: chr 4
allele count: 1
allele frequency: 8.697164724299877e-6
allele num: 114980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2034+15G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+856G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.723+15G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+847G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+847G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+856G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+856G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2034+15G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1872C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1872C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.723+15G>A
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19668
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

4-15010070-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010070
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010070
    reference: chr 4
allele count: 1
allele frequency: 8.80467704444601e-6
allele num: 113576
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1876T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+860A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+851A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+851A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2034+19A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.723+19A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2034+19A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.723+19A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+860A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1876T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+860A>G
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18326
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2582
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

4-15010072-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010072
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010072
    reference: chr 4
allele count: 3
allele frequency: 2.664629705291955e-5
allele num: 112586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.723+21T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+853T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+862T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+862T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+862T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2034+21T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1878A>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+853T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.723+21T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2034+21T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1878A>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17005
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6966
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 4.75e1
  variant carriers: 0
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: T
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

4-15010079-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010079
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010079
    reference: chr 4
allele count: 1
allele frequency: 9.01599437401951e-6
allele num: 110914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+869G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.723+28G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+860G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1885C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1885C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+860G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+869G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2034+28G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2034+28G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.723+28G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+869G>T
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13240
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17403
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

4-15010084-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010084
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010084
    reference: chr 4
allele count: 3
allele frequency: 2.752142083921986e-5
allele num: 109006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.723+33C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.723+33C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+865C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2034+33C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1890G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+865C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+874C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2034+33C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+874C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+874C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1890G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9659
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7872
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14843
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

4-15010085-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010085
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010085
    reference: chr 4
allele count: 8
allele frequency: 7.379256908829281e-5
allele num: 108412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2034+34G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+866G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+875G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.723+34G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+875G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2034+34G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1891C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.723+34G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+875G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1891C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+866G>A
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8597
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21912
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

4-15010085-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010085
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010085
    reference: chr 4
allele count: 3
allele frequency: 2.76722134081098e-5
allele num: 108412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2034+34G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2034+34G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+866G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.723+34G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+875G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1891C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+875G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+866G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+875G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.723+34G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1891C>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21912
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8597
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19272
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5091
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

4-15010094-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15010094
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15010094
    reference: chr 4
allele count: 1
allele frequency: 9.795470574406395e-6
allele num: 102088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.642+875T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.220+884T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.633+884T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.315-1900A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.414-1900A>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.633+884T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.723+43T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2034+43T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2034+43T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1953+875T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.723+43T>A
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13532
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

4-15018765-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018765
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018766
    reference: chr 4
allele count: 1
allele frequency: 8.814300320840532e-6
allele num: 113452
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-41dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-41dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-41dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+660dupT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-41dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-41dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-41dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-41dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-41dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-41dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+660dupT
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14681
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9916
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1802
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/4-15018769-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018769
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018769
    reference: chr 4
allele count: 1
allele frequency: 8.765010079761592e-6
allele num: 114090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-43A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-43A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-43A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-43A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-43A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-43A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-43A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-43A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-43A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+657T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+657T>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6563
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/4-15018770-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018770
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018770
    reference: chr 4
allele count: 28
allele frequency: 2.454245845312391e-4
allele num: 114088
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-42A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-42A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+656T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-42A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-42A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-42A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+656T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-42A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-42A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-42A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-42A>C
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14224
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18965
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5807
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6282
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3219
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-15018776-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018776
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018776
    reference: chr 4
allele count: 12
allele frequency: 1.048327916972429e-4
allele num: 114468
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+650T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+650T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-36A>G
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23232
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6176
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6464
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

4-15018777-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018777
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018777
    reference: chr 4
allele count: 2
allele frequency: 1.745931978490118e-5
allele num: 114552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-35T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-35T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-35T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-35T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-35T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+649A>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-35T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+649A>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-35T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-35T>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-35T>A
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5837
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

4-15018782-TATA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018782
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018779
    reference: chr 4
allele count: 4
allele frequency: 3.47252365656741e-5
allele num: 115190
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+641_234+643delTAT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+641_333+643delTAT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-27_221-25delAAT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-27_634-25delAAT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-27_1954-25delAAT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-27_724-25delAAT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-27_643-25delAAT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-27_2035-25delAAT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-27_2035-25delAAT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-27_724-25delAAT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-27_634-25delAAT
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: TATA
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

4-15018786-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018786
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018787
    reference: chr 4
allele count: 1
allele frequency: 8.633491038436302e-6
allele num: 115828
alternate allele: AT
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+639dupA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-25dupT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-25dupT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-25dupT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+639dupA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-25dupT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-25dupT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-25dupT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-25dupT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-25dupT
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-25dupT
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

4-15018786-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018786
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018786
    reference: chr 4
allele count: 1
allele frequency: 8.633491038436302e-6
allele num: 115828
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-26A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-26A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-26A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-26A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-26A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+640T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-26A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-26A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-26A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-26A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+640T>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15795
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2473
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

4-15018788-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018788
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018788
    reference: chr 4
allele count: 1
allele frequency: 8.611039352449841e-6
allele num: 116130
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-24G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-24G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-24G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-24G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+638C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-24G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-24G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+638C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-24G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-24G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-24G>T
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

4-15018789-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018789
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018789
    reference: chr 4
allele count: 1
allele frequency: 8.602002546192754e-6
allele num: 116252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-23T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-23T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-23T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-23T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-23T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+637A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-23T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-23T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-23T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-23T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+637A>C
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

4-15018790-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018790
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018790
    reference: chr 4
allele count: 1
allele frequency: 8.595348197555483e-6
allele num: 116342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-22C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+636G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-22C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-22C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-22C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-22C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-22C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-22C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-22C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-22C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+636G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

4-15018801-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018801
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018801
    reference: chr 4
allele count: 1
allele frequency: 8.461525443807009e-6
allele num: 118182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-11T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-11T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-11T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+625A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-11T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-11T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+625A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-11T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-11T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-11T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-11T>C
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-15018803-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018803
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018803
    reference: chr 4
allele count: 2
allele frequency: 1.688903901368012e-5
allele num: 118420
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-9C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+623G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+623G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-9C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-9C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-9C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-9C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-9C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-9C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-9C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-9C>G
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16920
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6899
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

4-15018807-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018807
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018807
    reference: chr 4
allele count: 1
allele frequency: 8.41609156707625e-6
allele num: 118820
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+619A>G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+619A>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-5T>C
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.2035-5T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

4-15018807-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018807
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018808
    reference: chr 4
allele count: 1
allele frequency: 8.41609156707625e-6
allele num: 118820
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+618dupG
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-3dupC
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-3dupC
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+618dupG
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-3dupC
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-3dupC
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-3dupC
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-3dupC
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-3dupC
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-3dupC
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-3dupC
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2035-3dupC
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/4-15018808-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018808
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018808
    reference: chr 4
allele count: 1
allele frequency: 8.410287463625507e-6
allele num: 118902
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.724-4C>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.634-4C>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1954-4C>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.643-4C>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.724-4C>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.634-4C>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+618G>T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2035-4C>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.221-4C>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2035-4C>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+618G>T
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17077
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.2035-4C>A
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP

4-15018822-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018822
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018822
    reference: chr 4
allele count: 1
allele frequency: 8.363581620193032e-6
allele num: 119566
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+604C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.734G>C
  hgvsp: ENSP00000424084.1:p.Arg245Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+604C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2045G>C
  hgvsp: ENSP00000437884.1:p.Arg682Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.644G>C
  hgvsp: ENSP00000371832.3:p.Arg215Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.644G>C
  hgvsp: ENSP00000334058.3:p.Arg215Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.734G>C
  hgvsp: ENSP00000259997.5:p.Arg245Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1964G>C
  hgvsp: ENSP00000414270.2:p.Arg655Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2045G>C
  hgvsp: ENSP00000443985.1:p.Arg682Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.653G>C
  hgvsp: ENSP00000371838.3:p.Arg218Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.231G>C
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg682Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

4-15018822-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018822
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018822
    reference: chr 4
allele count: 1
allele frequency: 8.363581620193032e-6
allele num: 119566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.231G>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1964G>T
  hgvsp: ENSP00000414270.2:p.Arg655Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2045G>T
  hgvsp: ENSP00000437884.1:p.Arg682Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.734G>T
  hgvsp: ENSP00000424084.1:p.Arg245Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.644G>T
  hgvsp: ENSP00000371832.3:p.Arg215Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.653G>T
  hgvsp: ENSP00000371838.3:p.Arg218Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+604C>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2045G>T
  hgvsp: ENSP00000443985.1:p.Arg682Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+604C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.644G>T
  hgvsp: ENSP00000334058.3:p.Arg215Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.734G>T
  hgvsp: ENSP00000259997.5:p.Arg245Ile
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg682Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

4-15018826-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018826
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018826
    reference: chr 4
allele count: 1
allele frequency: 8.355754608198667e-6
allele num: 119678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.657G>A
  hgvsp: ENSP00000371838.3:p.Met219Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2049G>A
  hgvsp: ENSP00000437884.1:p.Met683Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.738G>A
  hgvsp: ENSP00000424084.1:p.Met246Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.738G>A
  hgvsp: ENSP00000259997.5:p.Met246Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2049G>A
  hgvsp: ENSP00000443985.1:p.Met683Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.648G>A
  hgvsp: ENSP00000334058.3:p.Met216Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.648G>A
  hgvsp: ENSP00000371832.3:p.Met216Ile
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+600C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.235G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+600C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1968G>A
  hgvsp: ENSP00000414270.2:p.Met656Ile
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met683Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

4-15018848-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018848
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018848
    reference: chr 4
allele count: 1
allele frequency: 8.336668000533546e-6
allele num: 119952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.760T>C
  hgvsp: ENSP00000259997.5:p.Ser254Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2071T>C
  hgvsp: ENSP00000437884.1:p.Ser691Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.679T>C
  hgvsp: ENSP00000371838.3:p.Ser227Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2071T>C
  hgvsp: ENSP00000443985.1:p.Ser691Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+578A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.760T>C
  hgvsp: ENSP00000424084.1:p.Ser254Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.670T>C
  hgvsp: ENSP00000371832.3:p.Ser224Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.257T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1990T>C
  hgvsp: ENSP00000414270.2:p.Ser664Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+578A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.670T>C
  hgvsp: ENSP00000334058.3:p.Ser224Pro
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser691Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

4-15018850-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018850
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018850
    reference: chr 4
allele count: 1
allele frequency: 8.33694600993764e-6
allele num: 119948
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+576A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.762T>C
  hgvsp: ENST00000259997.5:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.681T>C
  hgvsp: ENST00000382401.3:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.1992T>C
  hgvsp: ENST00000442003.2:c.1992T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+576A>G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2073T>C
  hgvsp: ENST00000538197.1:c.2073T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2073T>C
  hgvsp: ENST00000541112.1:c.2073T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.672T>C
  hgvsp: ENST00000382395.3:c.672T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.259T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.762T>C
  hgvsp: ENST00000507071.1:c.762T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.672T>C
  hgvsp: ENST00000345451.3:c.672T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser691Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/4-15018862-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018862
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018862
    reference: chr 4
allele count: 3
allele frequency: 2.504549932377152e-5
allele num: 119782
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2085C>A
  hgvsp: ENST00000541112.1:c.2085C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2004C>A
  hgvsp: ENST00000442003.2:c.2004C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+564G>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.684C>A
  hgvsp: ENST00000382395.3:c.684C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.271C>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.774C>A
  hgvsp: ENST00000507071.1:c.774C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2085C>A
  hgvsp: ENST00000538197.1:c.2085C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.693C>A
  hgvsp: ENST00000382401.3:c.693C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+564G>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.774C>A
  hgvsp: ENST00000259997.5:c.774C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.684C>A
  hgvsp: ENST00000345451.3:c.684C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser695Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

4-15018863-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018863
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018863
    reference: chr 4
allele count: 28
allele frequency: 2.338126492643252e-4
allele num: 119754
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2086C>G
  hgvsp: ENSP00000443985.1:p.Leu696Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.775C>G
  hgvsp: ENSP00000424084.1:p.Leu259Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.685C>G
  hgvsp: ENSP00000371832.3:p.Leu229Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+563G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.685C>G
  hgvsp: ENSP00000334058.3:p.Leu229Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.272C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.694C>G
  hgvsp: ENSP00000371838.3:p.Leu232Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2086C>G
  hgvsp: ENSP00000437884.1:p.Leu696Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.775C>G
  hgvsp: ENSP00000259997.5:p.Leu259Val
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+563G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2005C>G
  hgvsp: ENSP00000414270.2:p.Leu669Val
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 30590
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7060
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu696Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

4-15018868-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018868
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018868
    reference: chr 4
allele count: 2
allele frequency: 1.673080140538732e-5
allele num: 119540
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.690C>T
  hgvsp: ENST00000382395.3:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2091C>T
  hgvsp: ENST00000538197.1:c.2091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.277C>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.699C>T
  hgvsp: ENST00000382401.3:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.780C>T
  hgvsp: ENST00000259997.5:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.780C>T
  hgvsp: ENST00000507071.1:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2010C>T
  hgvsp: ENST00000442003.2:c.2010C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2091C>T
  hgvsp: ENST00000541112.1:c.2091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.690C>T
  hgvsp: ENST00000345451.3:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+558G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+558G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17965
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile697Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

4-15018869-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018869
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018869
    reference: chr 4
allele count: 1
allele frequency: 8.374227477515199e-6
allele num: 119414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.700G>A
  hgvsp: ENSP00000371838.3:p.Asp234Asn
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.781G>A
  hgvsp: ENSP00000424084.1:p.Asp261Asn
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2011G>A
  hgvsp: ENSP00000414270.2:p.Asp671Asn
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2092G>A
  hgvsp: ENSP00000437884.1:p.Asp698Asn
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.278G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+557C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.781G>A
  hgvsp: ENSP00000259997.5:p.Asp261Asn
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.691G>A
  hgvsp: ENSP00000334058.3:p.Asp231Asn
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.691G>A
  hgvsp: ENSP00000371832.3:p.Asp231Asn
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2092G>A
  hgvsp: ENSP00000443985.1:p.Asp698Asn
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+557C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp698Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

4-15018876-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018876
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018876
    reference: chr 4
allele count: 1
allele frequency: 8.392359595823962e-6
allele num: 119156
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.707T>C
  hgvsp: ENSP00000371838.3:p.Met236Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.788T>C
  hgvsp: ENSP00000259997.5:p.Met263Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2018T>C
  hgvsp: ENSP00000414270.2:p.Met673Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.698T>C
  hgvsp: ENSP00000334058.3:p.Met233Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.788T>C
  hgvsp: ENSP00000424084.1:p.Met263Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.698T>C
  hgvsp: ENSP00000371832.3:p.Met233Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+550A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.285T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2099T>C
  hgvsp: ENSP00000437884.1:p.Met700Thr
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+550A>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2099T>C
  hgvsp: ENSP00000443985.1:p.Met700Thr
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met700Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

4-15018881-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018881
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018881
    reference: chr 4
allele count: 1
allele frequency: 8.413825598223e-6
allele num: 118852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.703G>C
  hgvsp: ENSP00000371832.3:p.Ala235Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+545C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.793G>C
  hgvsp: ENSP00000424084.1:p.Ala265Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.712G>C
  hgvsp: ENSP00000371838.3:p.Ala238Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2104G>C
  hgvsp: ENSP00000443985.1:p.Ala702Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.290G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2023G>C
  hgvsp: ENSP00000414270.2:p.Ala675Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2104G>C
  hgvsp: ENSP00000437884.1:p.Ala702Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+545C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.703G>C
  hgvsp: ENSP00000334058.3:p.Ala235Pro
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.793G>C
  hgvsp: ENSP00000259997.5:p.Ala265Pro
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala702Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

4-15018886-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018886
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018886
    reference: chr 4
allele count: 2
allele frequency: 1.690245592684617e-5
allele num: 118326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2028G>A
  hgvsp: ENST00000442003.2:c.2028G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2109G>A
  hgvsp: ENST00000541112.1:c.2109G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+540C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2109G>A
  hgvsp: ENST00000538197.1:c.2109G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.708G>A
  hgvsp: ENST00000345451.3:c.708G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.295G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.798G>A
  hgvsp: ENST00000507071.1:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.717G>A
  hgvsp: ENST00000382401.3:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.708G>A
  hgvsp: ENST00000382395.3:c.708G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.798G>A
  hgvsp: ENST00000259997.5:c.798G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+540C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu703Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

4-15018888-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018888
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018888
    reference: chr 4
allele count: 1
allele frequency: 8.472852979055108e-6
allele num: 118024
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+538T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2030A>G
  hgvsp: ENSP00000414270.2:p.His677Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.800A>G
  hgvsp: ENSP00000424084.1:p.His267Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.297A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.719A>G
  hgvsp: ENSP00000371838.3:p.His240Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2111A>G
  hgvsp: ENSP00000437884.1:p.His704Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.800A>G
  hgvsp: ENSP00000259997.5:p.His267Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+538T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2111A>G
  hgvsp: ENSP00000443985.1:p.His704Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.710A>G
  hgvsp: ENSP00000334058.3:p.His237Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.710A>G
  hgvsp: ENSP00000371832.3:p.His237Arg
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7059
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His704Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

4-15018902-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018902
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018902
    reference: chr 4
allele count: 1
allele frequency: 8.9394264463992e-6
allele num: 111864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125G>A
  hgvsp: ENSP00000437884.1:p.Gly709Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814G>A
  hgvsp: ENSP00000424084.1:p.Gly272Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044G>A
  hgvsp: ENSP00000414270.2:p.Gly682Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724G>A
  hgvsp: ENSP00000371832.3:p.Gly242Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+524C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814G>A
  hgvsp: ENSP00000259997.5:p.Gly272Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125G>A
  hgvsp: ENSP00000443985.1:p.Gly709Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.311G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733G>A
  hgvsp: ENSP00000371838.3:p.Gly245Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724G>A
  hgvsp: ENSP00000334058.3:p.Gly242Ser
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+524C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20696
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly709Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD

4-15018902-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018902
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018902
    reference: chr 4
allele count: 1
allele frequency: 8.9394264463992e-6
allele num: 111864
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044G>C
  hgvsp: ENSP00000414270.2:p.Gly682Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125G>C
  hgvsp: ENSP00000437884.1:p.Gly709Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724G>C
  hgvsp: ENSP00000334058.3:p.Gly242Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814G>C
  hgvsp: ENSP00000259997.5:p.Gly272Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814G>C
  hgvsp: ENSP00000424084.1:p.Gly272Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125G>C
  hgvsp: ENSP00000443985.1:p.Gly709Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733G>C
  hgvsp: ENSP00000371838.3:p.Gly245Arg
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+524C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.311G>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+524C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724G>C
  hgvsp: ENSP00000371832.3:p.Gly242Arg
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly709Arg
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

4-15018907-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018907
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018907
    reference: chr 4
allele count: 20
allele frequency: 1.885938442969221e-4
allele num: 106048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724+5G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125+5G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724+5G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125+5G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814+5G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044+5G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+519C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814+5G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.316G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733+5G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+519C>T
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14655
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11107
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6845
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: c.2125+5G>A
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ

4-15018916-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018916
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018917
    reference: chr 4
allele count: 7
allele frequency: 7.403177020538528e-5
allele num: 94554
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733+21dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125+21dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+509dupT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724+21dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125+21dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814+21dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.332dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+509dupT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044+21dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814+21dupA
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724+21dupA
  variant of: http://identifiers.org/hgnc/21745
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17959
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7192
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17217
  bin: 6.25e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-15018917-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018917
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018917
    reference: chr 4
allele count: 18
allele frequency: 1.904520060944642e-4
allele num: 94512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733+15A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+509T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125+15A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.326A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724+15A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+509T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814+15A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724+15A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814+15A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044+15A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125+15A>T
  variant of: http://identifiers.org/hgnc/21745
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7200
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4830
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10962
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17984
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/4-15018923-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018923
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018923
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 81978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814+21A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733+21A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+503T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724+21A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125+21A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814+21A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+503T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044+21A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.332A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125+21A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724+21A>C
  variant of: http://identifiers.org/hgnc/21745
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13345
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3771
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-15018925-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018925
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018925
    reference: chr 4
allele count: 1
allele frequency: 1.219125643088777e-5
allele num: 82026
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+501T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814+23A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724+23A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724+23A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.334A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125+23A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733+23A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814+23A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044+23A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+501T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125+23A>G
  variant of: http://identifiers.org/hgnc/21745
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5632
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

4-15018926-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018926
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018926
    reference: chr 4
allele count: 6
allele frequency: 7.317787101180602e-5
allele num: 81992
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.335T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125+24T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814+24T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044+24T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733+24T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724+24T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125+24T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+500A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814+24T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+500A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724+24T>C
  variant of: http://identifiers.org/hgnc/21745
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21587
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

4-15018927-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018927
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018927
    reference: chr 4
allele count: 296
allele frequency: 3.606062082744505e-3
allele num: 82084
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+499T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724+25A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+499T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814+25A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.336A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733+25A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125+25A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044+25A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724+25A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814+25A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125+25A>T
  variant of: http://identifiers.org/hgnc/21745
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21590
  bin: 1.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 2.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 13620
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 2.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 1.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1623
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 8.75e1
  variant carriers: 2
num of homozygotes: 3
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: A
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-15018933-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018933
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018933
    reference: chr 4
allele count: 52
allele frequency: 6.936848002988181e-4
allele num: 74962
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724+31A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814+31A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125+31A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.342A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125+31A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+493T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724+31A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044+31A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+493T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733+31A>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814+31A>C
  variant of: http://identifiers.org/hgnc/21745
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15313
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6963
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5466
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20577
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4536
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4100
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD

4-15018935-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018935
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018935
    reference: chr 4
allele count: 2
allele frequency: 2.798690212980325e-5
allele num: 71462
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814+33A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.344A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724+33A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044+33A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724+33A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125+33A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814+33A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733+33A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+491T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+491T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125+33A>G
  variant of: http://identifiers.org/hgnc/21745
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7644
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

4-15018938-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018938
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018938
    reference: chr 4
allele count: 1
allele frequency: 1.433198612663743e-5
allele num: 69774
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+488T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724+36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044+36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733+36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125+36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.347A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814+36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814+36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724+36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125+36A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+488T>C
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18749
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1726
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4107
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

4-15018938-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15018938
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15018938
    reference: chr 4
allele count: 1
allele frequency: 1.433198612663743e-5
allele num: 69774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.724+36A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2125+36A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.814+36A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.333+488T>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2125+36A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2044+36A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.234+488T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137449
  ensembl transcript: ENST00000503926
  gene symbol: CPEB2
  hgvsc: ENST00000503926.1:n.347A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.814+36A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.724+36A>T
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.733+36A>T
  variant of: http://identifiers.org/hgnc/21745
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2901
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum

4-15034734-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15034734
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15034734
    reference: chr 4
allele count: 1
allele frequency: 8.348917980229763e-6
allele num: 119776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.725-51T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2045-51T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.725-51T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2126-51T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.155-15229A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2126-51T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.815-51T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.734-51T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.815-51T>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.254-15229A>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8205
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7406
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2850
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum

4-15034740-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15034740
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15034740
    reference: chr 4
allele count: 3
allele frequency: 2.500666844491865e-5
allele num: 119968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2045-45A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.815-45A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2126-45A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.155-15235T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.815-45A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.725-45A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.725-45A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.734-45A>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.254-15235T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2126-45A>G
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6209
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32384
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

4-15034750-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15034750
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15034750
    reference: chr 4
allele count: 1
allele frequency: 8.323483877411729e-6
allele num: 120142
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.155-15245A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2126-35T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2126-35T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.254-15245A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.725-35T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.734-35T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.815-35T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.725-35T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2045-35T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.815-35T>C
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

4-15034770-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15034770
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15034770
    reference: chr 4
allele count: 2
allele frequency: 1.658374792703151e-5
allele num: 120600
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.734-15C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.815-15C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2126-15C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.725-15C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2045-15C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.155-15265G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2126-15C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.725-15C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.815-15C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.254-15265G>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

4-15034773-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15034773
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15034773
    reference: chr 4
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.155-15268C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.815-12G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2126-12G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2045-12G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.725-12G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.254-15268C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2126-12G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.725-12G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.815-12G>A
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.734-12G>A
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7421
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

4-15034775-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15034775
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15034775
    reference: chr 4
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2126-10C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.254-15270G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.815-10C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.734-10C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2126-10C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.725-10C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2045-10C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.155-15270G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.725-10C>G
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.815-10C>G
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2115
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

4-15034780-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 15034780
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 15034780
    reference: chr 4
allele count: 2
allele frequency: 1.657247974014352e-5
allele num: 120682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000437884
  ensembl transcript: ENST00000541112
  gene symbol: CPEB2
  hgvsc: ENST00000541112.1:c.2126-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000259997
  ensembl transcript: ENST00000259997
  gene symbol: CPEB2
  hgvsc: ENST00000259997.5:c.815-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000334058
  ensembl transcript: ENST00000345451
  gene symbol: CPEB2
  hgvsc: ENST00000345451.3:c.725-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371838
  ensembl transcript: ENST00000382401
  gene symbol: CPEB2
  hgvsc: ENST00000382401.3:c.734-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000513384
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000513384.1:n.254-15275A>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000249252
  ensembl transcript: ENST00000502344
  gene symbol: RP11-665G4.1
  hgvsc: ENST00000502344.1:n.155-15275A>G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000443985
  ensembl transcript: ENST00000538197
  gene symbol: CPEB2
  hgvsc: ENST00000538197.1:c.2126-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000424084
  ensembl transcript: ENST00000507071
  gene symbol: CPEB2
  hgvsc: ENST00000507071.1:c.815-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000414270
  ensembl transcript: ENST00000442003
  gene symbol: CPEB2
  hgvsc: ENST00000442003.2:c.2045-5T>C
  variant of: http://identifiers.org/hgnc/21745
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137449
  ensembl protein: ENSP00000371832
  ensembl transcript: ENST00000382395
  gene symbol: CPEB2
  hgvsc: ENST00000382395.3:c.725-5T>C
  variant of: http://identifiers.org/hgnc/21745
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38899
  bin: 6.25e1
  variant carriers: 0
hgvs: c.2126-5T>C
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 744
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45559
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 170
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1498
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 4
allele frequency: 3.498338289312576e-4
allele num: 11434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
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: 4
allele frequency: 6.02918123718799e-5
allele num: 66344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16338
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.073e0

FS
type: SiteQuality
SIO_000300: 1.506e0

QD
type: SiteQuality
SIO_000300: 1.45e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 1.620118e6

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

GenotypeQuality
all individuals: 1513
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46190
bin: 6.25e1
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: 1073
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2598
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1332
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5955
bin: 6.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.009e0

DP
type: SiteQuality
SIO_000300: 1.62997e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.89e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.034e0

FS
type: SiteQuality
SIO_000300: 1.4856e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.14e0

QD
type: SiteQuality
SIO_000300: 1.509e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.92e-1

GenotypeQuality
all individuals: 2599
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1335
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1523
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5986
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46415
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.632618e6

FS
type: SiteQuality
SIO_000300: 4.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.04e-1

QD
type: SiteQuality
SIO_000300: 1.234e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.749000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

MQ
type: SiteQuality
SIO_000300: 5.878e1

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

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1528
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2602
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46453
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5991
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.040622719532961e-4
allele num: 16444
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: 6612
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.634133e6

MQ
type: SiteQuality
SIO_000300: 5.94e1

FS
type: SiteQuality
SIO_000300: 5.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.574e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

QD
type: SiteQuality
SIO_000300: 1.146e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 1074
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46458
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2600
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5999
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1529
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 458
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
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: 10360
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.389999999999999e-1

FS
type: SiteQuality
SIO_000300: 5.159e0

VQSLOD
type: SiteQuality
SIO_000300: -6.271e-1

QD
type: SiteQuality
SIO_000300: 6.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.634654e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 46427
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6003
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 746
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
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: 11520
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.0790273556231e-5
allele num: 16450
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: 66624
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.536e0

DP
type: SiteQuality
SIO_000300: 1.635056e6

MQ
type: SiteQuality
SIO_000300: 5.978e1

QD
type: SiteQuality
SIO_000300: 1.233e1

MQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 1.815e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-1

GenotypeQuality
all individuals: 1522
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46432
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1076
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5995
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.663703131039814e-5
allele num: 10348
num of homozygotes: 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: 66626
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: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 1.895e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

QD
type: SiteQuality
SIO_000300: 1.088e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

DP
type: SiteQuality
SIO_000300: 1.635184e6

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

GenotypeQuality
all individuals: 2602
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.502881844380403e-5
allele num: 66624
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.667440061871617e-5
allele num: 10344
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.635165e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.47e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e-1

FS
type: SiteQuality
SIO_000300: 5.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

GenotypeQuality
all individuals: 688
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
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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
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
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: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66366
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.113964294448521e-5
allele num: 16356
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.33e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.077e0

FS
type: SiteQuality
SIO_000300: 3.135e0

QD
type: SiteQuality
SIO_000300: 9.130000000000001e0

DP
type: SiteQuality
SIO_000300: 1.629631e6

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 4
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2595
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variant carriers: 1

GenotypeQuality
all individuals: 456
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508932882665379e-5
allele num: 66272
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: 10294
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

MQRankSum
type: SiteQuality
SIO_000300: 9.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.702e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.627959e6

VQSLOD
type: SiteQuality
SIO_000300: -1.424e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.867e0

QD
type: SiteQuality
SIO_000300: 8.09e0

GenotypeQuality
all individuals: 734
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 29
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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
all individuals: 2592
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variant carriers: 9

GenotypeQuality
all individuals: 246
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.425449016440179e-4
allele num: 63138
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10922
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.15e-1

DP
type: SiteQuality
SIO_000300: 1.524102e6

VQSLOD
type: SiteQuality
SIO_000300: 2.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.763e0

QD
type: SiteQuality
SIO_000300: 1.294e1

GenotypeQuality
all individuals: 1340
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5037
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GenotypeQuality
all individuals: 1082
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.594031944400166e-5
allele num: 62734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.276e0

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

QD
type: SiteQuality
SIO_000300: 5.95e0

DP
type: SiteQuality
SIO_000300: 1.506031e6

VQSLOD
type: SiteQuality
SIO_000300: -6.168e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1687
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61838
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.210067763794773e-4
allele num: 8264
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

FS
type: SiteQuality
SIO_000300: 2.0031e1

MQRankSum
type: SiteQuality
SIO_000300: 9.11e-1

DP
type: SiteQuality
SIO_000300: 1.453664e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.54e0

VQSLOD
type: SiteQuality
SIO_000300: -2.838e0

QD
type: SiteQuality
SIO_000300: 1.384e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 947
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15666
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.902120984345894e-5
allele num: 61198
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.236e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.25e0

QD
type: SiteQuality
SIO_000300: 2.379e1

DP
type: SiteQuality
SIO_000300: 1.407364e6

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
all individuals: 428
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GenotypeQuality
all individuals: 178
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 834
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.661129568106312e-5
allele num: 60200
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ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -4.367e0

VQSLOD
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InbreedingCoeff
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SIO_000300: -2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.19e-1

QD
type: SiteQuality
SIO_000300: 7.87e0

DP
type: SiteQuality
SIO_000300: 1.299095e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 9450
num of homozygotes: 0

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

South Asian
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allele frequency: 6.502796202367018e-5
allele num: 15378
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.693709562684191e-5
allele num: 59042
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6198
num of homozygotes: 0

Latino
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allele frequency: 9.748488984207447e-5
allele num: 10258
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

FS
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MQ
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MQRankSum
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InbreedingCoeff
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SIO_000300: -3.6e-3

VQSLOD
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DP
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6174
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.192951361668768e-4
allele num: 58678
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.063603488619443e-4
allele num: 9402
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ClippingRankSum
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DP
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BaseQRankSum
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VQSLOD
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MQ
type: SiteQuality
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FS
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QD
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MQRankSum
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SIO_000300: 2.1e-2

InbreedingCoeff
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SIO_000300: 4.0e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6174
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 5.112648692866151e-5
allele num: 58678
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

BaseQRankSum
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SIO_000300: -1.551e0

InbreedingCoeff
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SIO_000300: 4.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.365e0

DP
type: SiteQuality
SIO_000300: 1.19229e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14872
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.835401218706409e-5
allele num: 54484
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9670
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5952
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

ClippingRankSum
type: SiteQuality
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FS
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

QD
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VQSLOD
type: SiteQuality
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DP
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.341154090044388e-5
allele num: 15770
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61822
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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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: 8078
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

VQSLOD
type: SiteQuality
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FS
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BaseQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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African
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FS
type: SiteQuality
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InbreedingCoeff
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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allele frequency: 3.197245450073783e-3
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Latino
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South Asian
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European (Finnish)
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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: 2
allele frequency: 3.21450384133209e-5
allele num: 62218
num of homozygotes: 0

MQ
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FS
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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QD
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InbreedingCoeff
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SIO_000300: 1.4e-3

BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 9.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.201229272040464e-5
allele num: 62476
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.305965443309371e-4
allele num: 15858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.587e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.37e-1

QD
type: SiteQuality
SIO_000300: 1.011e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.902e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.451751e6

GenotypeQuality
all individuals: 111
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5193
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2374
bin: 3.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15864
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6408
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.442598925256473e-4
allele num: 8188
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.98e-1

DP
type: SiteQuality
SIO_000300: 1.457342e6

MQRankSum
type: SiteQuality
SIO_000300: -8.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

FS
type: SiteQuality
SIO_000300: 2.515e0

MQ
type: SiteQuality
SIO_000300: 5.747e1

VQSLOD
type: SiteQuality
SIO_000300: -1.697e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 8.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
all individuals: 2735
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.355662895640016e-5
allele num: 62936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6418
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 1.486483e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.88e-1

FS
type: SiteQuality
SIO_000300: 8.97e-1

MQ
type: SiteQuality
SIO_000300: 5.566e1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

QD
type: SiteQuality
SIO_000300: 1.62e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.3e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.28e-1

GenotypeQuality
all individuals: 2473
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1022
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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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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10950
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15936
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.579030475288173e-5
allele num: 63330
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

FS
type: SiteQuality
SIO_000300: 5.349e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

DP
type: SiteQuality
SIO_000300: 1.506255e6

QD
type: SiteQuality
SIO_000300: 7.37e0

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
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GenotypeQuality
all individuals: 1000
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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
all individuals: 231
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9972
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10950
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.579030475288173e-5
allele num: 63330
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e0

DP
type: SiteQuality
SIO_000300: 1.506255e6

QD
type: SiteQuality
SIO_000300: 7.37e0

FS
type: SiteQuality
SIO_000300: 5.349e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

GenotypeQuality
all individuals: 1260
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
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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: 5.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1054
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.57400994774287e-5
allele num: 63532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10972
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.257e0

QD
type: SiteQuality
SIO_000300: 9.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-2

DP
type: SiteQuality
SIO_000300: 1.514218e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQ
type: SiteQuality
SIO_000300: 5.698e1

FS
type: SiteQuality
SIO_000300: 2.695e0

MQRankSum
type: SiteQuality
SIO_000300: -9.379999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.501e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 188
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63592
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.193887297039159e-4
allele num: 8376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10988
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.516681e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.56e-1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 15974
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10984
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.570993181889591e-5
allele num: 63654
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.296e0

DP
type: SiteQuality
SIO_000300: 1.522318e6

FS
type: SiteQuality
SIO_000300: 1.4546e1

MQ
type: SiteQuality
SIO_000300: 5.713e1

QD
type: SiteQuality
SIO_000300: 9.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.077e0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
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GenotypeQuality
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GenotypeQuality
all individuals: 1069
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11096
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.540927021696253e-5
allele num: 64896
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e0

DP
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QD
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MQ
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MQRankSum
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SIO_000300: 7.35e-1

VQSLOD
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SIO_000300: -2.115e-1

FS
type: SiteQuality
SIO_000300: 9.11e-1

BaseQRankSum
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SIO_000300: 8.149999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.235788433020267e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65046
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6494
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11120
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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FS
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QD
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BaseQRankSum
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SIO_000300: 2.94e0

DP
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MQ
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SIO_000300: 5.978e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.531252871099133e-5
allele num: 65306
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
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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 count: 0
allele frequency: 0.0e0
allele num: 11140
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

East Asian
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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FS
type: SiteQuality
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MQ
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DP
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VQSLOD
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MQRankSum
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SIO_000300: -2.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.72e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531252871099133e-5
allele num: 65306
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16244
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

MQ
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SIO_000300: 6.05e1

QD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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DP
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SIO_000300: 1.565339e6

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11152
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.530128224745234e-5
allele num: 65354
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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MQ
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QD
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DP
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SIO_000300: 1.566853e6

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

South Asian
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allele num: 16316
num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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Other
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African
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FS
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VQSLOD
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DP
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QD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65850
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.92379082634303e-5
allele num: 11206
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.97e0

MQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

FS
type: SiteQuality
SIO_000300: 2.611e0

VQSLOD
type: SiteQuality
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DP
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SIO_000300: 1.578892e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.309e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1108
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GenotypeQuality
all individuals: 191
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11224
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.514738404677512e-5
allele num: 66018
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
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SIO_000300: 8.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: -7.38e-1

DP
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SIO_000300: 1.583947e6

FS
type: SiteQuality
SIO_000300: 1.0797e1

InbreedingCoeff
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SIO_000300: -3.0e-4

VQSLOD
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SIO_000300: -2.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.455e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11224
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.701202949165696e-5
allele num: 10308
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.236e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

DP
type: SiteQuality
SIO_000300: 1.583782e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 948
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1046
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GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
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: 0
allele frequency: 0.0e0
allele num: 11208
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.551108953548348e-5
allele num: 65918
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.184e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.519e0

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.582182e6

QD
type: SiteQuality
SIO_000300: 1.189e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.237e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

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

GenotypeQuality
all individuals: 106
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GenotypeQuality
all individuals: 37
bin: 4.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1102
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GenotypeQuality
all individuals: 1804
bin: 9.75e1
variant carriers: 28

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 3.642102707296346e-4
allele num: 65896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.570153516601214e-4
allele num: 11204
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

BaseQRankSum
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SIO_000300: -1.289e0

DP
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SIO_000300: 1.582552e6

ClippingRankSum
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SIO_000300: -1.83e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
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: 1
allele frequency: 1.165772907437631e-4
allele num: 8578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521282745611099e-5
allele num: 65734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11196
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
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VQSLOD
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MQRankSum
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DP
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FS
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ReadPosRankSum
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SIO_000300: 2.3e-1

MQ
type: SiteQuality
SIO_000300: 5.669e1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166316771635176e-4
allele num: 8574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65632
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.9e-2

FS
type: SiteQuality
SIO_000300: 8.48e-1

BaseQRankSum
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SIO_000300: -8.129999999999999e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 47847
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527557130636686e-5
allele num: 65464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.78e-1

FS
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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QD
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10258
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.169031462060457e-5
allele num: 16210
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65258
num of homozygotes: 0

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

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

Other
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ClippingRankSum
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SIO_000300: -1.846e0

MQRankSum
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MQ
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SIO_000300: 5.933e1

FS
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SIO_000300: 1.636e0

InbreedingCoeff
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SIO_000300: -7.0e-4

DP
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BaseQRankSum
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SIO_000300: -1.24e-1

QD
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SIO_000300: 1.233e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e-1

VQSLOD
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SIO_000300: 1.47e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8528
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.08090455357693e-5
allele num: 64916
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10236
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: -7.0e-4

QD
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FS
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SIO_000300: 2.422e0

BaseQRankSum
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SIO_000300: -5.11e0

MQ
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MQRankSum
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SIO_000300: -3.09e-1

ReadPosRankSum
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SIO_000300: 2.33e0

VQSLOD
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SIO_000300: 2.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.7e-1

DP
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SIO_000300: 1.560748e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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VQSLOD
type: SiteQuality
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FS
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SIO_000300: 3.952e0

QD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -7.0e-4

DP
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SIO_000300: 1.556134e6

MQ
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SIO_000300: 5.883e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.653493832468005e-5
allele num: 60478
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: 5.639999999999999e-1

ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.1e-3

MQ
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DP
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VQSLOD
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SIO_000300: 1.02e0

MQRankSum
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SIO_000300: 1.02e-1

FS
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SIO_000300: 1.709e0

QD
type: SiteQuality
SIO_000300: 1.251e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60478
num of homozygotes: 0

South Asian
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allele num: 15556
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MQRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

African
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Other
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Latino
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European (Finnish)
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East Asian
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European (Non-Finnish)
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allele frequency: 3.521002781592198e-4
allele num: 56802
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QD
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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FS
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DP
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 1.164958061509786e-4
allele num: 8584
num of homozygotes: 0

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

Other
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European (Non-Finnish)
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allele frequency: 1.199184554502938e-4
allele num: 50034
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European (Finnish)
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ClippingRankSum
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QD
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VQSLOD
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FS
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MQ
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DP
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 2
allele frequency: 1.415428167020524e-4
allele num: 14130
num of homozygotes: 0

African
type: Population
allele count: 15
allele frequency: 1.749475157452764e-3
allele num: 8574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.999280259106722e-5
allele num: 50018
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.61e-1

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.347e0

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 1.051e0

DP
type: SiteQuality
SIO_000300: 1.145817e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5202
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.63835e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

FS
type: SiteQuality
SIO_000300: 3.522e0

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

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4916
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5202
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.355268736162796e-5
allele num: 42458
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 9.60227e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.451e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.44e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
all individuals: 229
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GenotypeQuality
all individuals: 291
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 6.154603643525357e-4
allele num: 8124
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5202
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.35626767200754e-5
allele num: 42440
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

DP
type: SiteQuality
SIO_000300: 9.5886e5

MQRankSum
type: SiteQuality
SIO_000300: 6.46e-1

FS
type: SiteQuality
SIO_000300: 6.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

VQSLOD
type: SiteQuality
SIO_000300: -2.349e0

QD
type: SiteQuality
SIO_000300: 2.488e1

GenotypeQuality
all individuals: 3701
bin: 2.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 283

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 912
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variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13120
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4906
num of homozygotes: 0

African
type: Population
allele count: 275
allele frequency: 3.650119458455004e-2
allele num: 7534
num of homozygotes: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5186
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.408222786715589e-5
allele num: 42516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

Latino
type: Population
allele count: 17
allele frequency: 2.090506640432858e-3
allele num: 8132
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-3

QD
type: SiteQuality
SIO_000300: 1.524e1

DP
type: SiteQuality
SIO_000300: 9.57455e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7018
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7598
num of homozygotes: 0

European (Finnish)
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allele count: 13
allele frequency: 2.849627356422622e-3
allele num: 4562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 39
allele frequency: 1.022870331514897e-3
allele num: 38128
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.75639e5

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.674e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
allele frequency: 0.0e0
allele num: 12258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6794
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7310
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 4.914004914004914e-4
allele num: 4070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36006
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

BaseQRankSum
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InbreedingCoeff
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DP
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.102e0

ClippingRankSum
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.235e1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.853718395068775e-5
allele num: 35042
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7162
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

DP
type: SiteQuality
SIO_000300: 8.29357e5

FS
type: SiteQuality
SIO_000300: 1.453e0

BaseQRankSum
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SIO_000300: 2.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.57e-2

VQSLOD
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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Other
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East Asian
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allele frequency: 2.592016588906169e-4
allele num: 3858
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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VQSLOD
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QD
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.519664458087654e-5
allele num: 65804
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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VQSLOD
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FS
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DP
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.516484183069971e-5
allele num: 65942
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 1.944768572539868e-4
allele num: 10284
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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ClippingRankSum
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QD
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VQSLOD
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DP
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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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 count: 0
allele frequency: 0.0e0
allele num: 66072
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

African
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allele frequency: 9.718172983479106e-5
allele num: 10290
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 902
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16356
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.914337e6

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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QD
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MQRankSum
type: SiteQuality
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VQSLOD
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MQ
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SIO_000300: 5.942e1

ReadPosRankSum
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SIO_000300: 9.3e-1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 5.965e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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allele frequency: 0.0e0
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Other
type: Population
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 2
allele frequency: 1.936483346243222e-4
allele num: 10328
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66356
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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ReadPosRankSum
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DP
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16408
num of homozygotes: 0

European (Non-Finnish)
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African
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Latino
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European (Finnish)
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Other
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East Asian
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.506205566935775e-5
allele num: 66392
num of homozygotes: 0

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