17-27944280-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944280
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944280
    reference: chr 17
allele count: 1
allele frequency: 6.38895987733197e-5
allele num: 15652
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-415A>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.31A>T
  hgvsp: ENSP00000403019.3:p.Thr11Ser
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.*61A>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.719A>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2218A>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.754-220A>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-220A>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.208A>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.2065A>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.754-220A>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-220A>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-220A>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56563T>A
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33812
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr11Ser
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

17-27944282-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944282
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944282
    reference: chr 17
allele count: 1
allele frequency: 6.697026520225021e-5
allele num: 14932
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-222T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.754-222T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.717T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2216T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-417T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.2063T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.*59T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-222T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-222T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.29T>C
  hgvsp: ENSP00000403019.3:p.Val10Ala
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.754-222T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56565A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.206T>C
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33939
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val10Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-27944289-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944289
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944289
    reference: chr 17
allele count: 1
allele frequency: 7.267441860465116e-5
allele num: 13760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.22T>G
  hgvsp: ENSP00000403019.3:p.Phe8Val
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-229T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.*52T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-229T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2209T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.2056T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.710T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-424T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.199T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+229T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56572A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+229T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-229T>G
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34591
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3279
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe8Val
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

17-27944299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944299
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944299
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 12338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-239C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.700C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-434C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56582G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-239C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+219C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2199C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.*42C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.2046C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-239C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.12C>T
  hgvsp: ENST00000456796.3:c.12C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+219C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.189C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34937
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro4Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

17-27944309-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944309
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944309
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 11336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.2T>A
  hgvsp: ENSP00000403019.3:p.Met1?
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.179T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-249T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-249T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-249T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.*32T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+209T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.2036T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2189T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+209T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.690T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-444T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56592A>T
canonical: false
consequence: start lost
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 34388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14439
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-27944317-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944317
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944317
    reference: chr 17
allele count: 3
allele frequency: 2.797463632972771e-4
allele num: 10724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-452C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-257C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56600G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.2028C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.171C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.682C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.*24C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2181C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-257C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-7C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+201C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+201C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-257C>A
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33158
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17025
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

17-27944319-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944319
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944319
    reference: chr 17
allele count: 4
allele frequency: 3.818980332251289e-4
allele num: 10474
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.169C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.*22C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.2026C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-454C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.680C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+199C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56602G>C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-9C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-259C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-259C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+199C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2179C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-259C>G
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32671
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17794
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS

17-27944325-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944325
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944325
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 10108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2173C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-265C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.2020C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-265C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-460C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-15C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+193C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-265C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.*16C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+193C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56608G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.163C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.674C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19904
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

17-27944331-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944331
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944331
    reference: chr 17
allele count: 1
allele frequency: 9.827044025157233e-5
allele num: 10176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-271C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.157C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56614G>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-21C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-466C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.668C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2167C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.*10C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-271C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.2014C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-271C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+187C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+187C>A
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23341
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28857
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

17-27944363-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944363
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944363
    reference: chr 17
allele count: 10
allele frequency: 5.719514985129262e-4
allele num: 17484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-498C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1982C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-303C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-5C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-303C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-5C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2135C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.641-5C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56646G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+155C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+155C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.125C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-303C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37891
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12279
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-48-5C>T
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/17-27944380-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944380
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944380
    reference: chr 17
allele count: 1
allele frequency: 2.87720105880999e-5
allele num: 34756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1965T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.108T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-320T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.641-22T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56663A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-515T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-320T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+138T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2118T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+138T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-320T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-22T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-22T>G
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7180
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP

17-27944391-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944391
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944391
    reference: chr 17
allele count: 2
allele frequency: 4.329004329004329e-5
allele num: 46200
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.641-33G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-331G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-33G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-33G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1954G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+127G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+127G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2107G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-526G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56674C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.97G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-331G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-331G>C
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 13410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27932
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

17-27944398-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944398
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944398
    reference: chr 17
allele count: 1
allele frequency: 1.630948886061911e-5
allele num: 61314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-338C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-338C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56681G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-533C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.641-40C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-338C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.90C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1947C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2100C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+120C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-40C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-40C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+120C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

17-27944402-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944402
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944402
    reference: chr 17
allele count: 1
allele frequency: 1.559429872438636e-5
allele num: 64126
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56685T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-537A>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2096A>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+116A>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-44A>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.641-44A>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1943A>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-342A>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-342A>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+116A>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-342A>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-44A>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.86A>C
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19532
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20535
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

17-27944468-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944468
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944468
    reference: chr 17
allele count: 1
allele frequency: 9.157844609692663e-6
allele num: 109196
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-408G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56751C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-408G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.640+28G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-110G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1877G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+50G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+50G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2030G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-408G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.20G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-110G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-603G>C
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-27944469-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944469
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944469
    reference: chr 17
allele count: 2
allele frequency: 1.832508704416346e-5
allele num: 109140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-409G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-604G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2029G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+49G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.19G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.640+27G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-409G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-111G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1876G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+49G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-111G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56752C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-409G>T
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

17-27944470-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944470
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944470
    reference: chr 17
allele count: 1
allele frequency: 9.15616759449165e-6
allele num: 109216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.18C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1875C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+48C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+48C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-112C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2028C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-410C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.640+26C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-112C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-410C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56753G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-605C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-410C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

17-27944477-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944477
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944477
    reference: chr 17
allele count: 1
allele frequency: 9.157173729900004e-6
allele num: 109204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1868G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-119G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-417G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+41G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.11G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-612G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.640+19G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56760C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-417G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+41G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2021G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-417G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-119G>C
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

17-27944485-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944485
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944485
    reference: chr 17
allele count: 1
allele frequency: 9.128751917037902e-6
allele num: 109544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2013C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+33C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-127C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.640+11C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-620C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-127C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000579388
  gene symbol: CORO6
  hgvsc: ENST00000579388.1:n.3C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1860C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-425C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56768G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-425C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-425C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+33C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

17-27944498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944498
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944498
    reference: chr 17
allele count: 1
allele frequency: 9.081332413091649e-6
allele num: 110116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-140G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1847G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56781C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.2000G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-438G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-438G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.638G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-438G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+20G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-633G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+20G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-140G>A
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.638G>A
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

17-27944499-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944499
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944499
    reference: chr 17
allele count: 1
allele frequency: 9.06240371196056e-6
allele num: 110346
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56782A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-439T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1999T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-634T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1846T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+19T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-439T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.637T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-439T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-141T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-141T>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+19T>C
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

17-27944500-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944500
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944500
    reference: chr 17
allele count: 1
allele frequency: 9.059448098421843e-6
allele num: 110382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-440T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.636T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.753+18T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-142T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.753+18T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1845T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-440T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1998T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56783A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-635T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-142T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-440T>A
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

17-27944519-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944519
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944519
    reference: chr 17
allele count: 30
allele frequency: 2.683699210992432e-4
allele num: 111786
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56802G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1826C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-459C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-459C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.752C>T
  hgvsp: ENSP00000344562.5:p.Pro251Leu
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.752C>T
  hgvsp: ENSP00000373419.3:p.Pro251Leu
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.617C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-459C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-654C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1979C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-161C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-161C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9191
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14762
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28288
  bin: 2.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Pro251Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-27944519-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944519
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944519
    reference: chr 17
allele count: 1
allele frequency: 8.94566403664144e-6
allele num: 111786
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.752C>G
  hgvsp: ENSP00000344562.5:p.Pro251Arg
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1979C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-161C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-459C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.617C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.752C>G
  hgvsp: ENSP00000373419.3:p.Pro251Arg
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-459C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-459C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-161C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1826C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56802G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-654C>G
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro251Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-27944520-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944520
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944520
    reference: chr 17
allele count: 11
allele frequency: 9.82669287118099e-5
allele num: 111940
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56803G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.751C>T
  hgvsp: ENSP00000373419.3:p.Pro251Ser
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-460C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.616C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1978C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-655C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-162C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.751C>T
  hgvsp: ENSP00000344562.5:p.Pro251Ser
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1825C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-460C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-460C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-162C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9168
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro251Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

17-27944529-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944529
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944529
    reference: chr 17
allele count: 1
allele frequency: 8.926977325477594e-6
allele num: 112020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-171C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-469C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1816C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.607C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.742C>T
  hgvsp: ENST00000388767.3:c.742C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-664C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.742C>T
  hgvsp: ENST00000345068.5:c.742C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56812G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-469C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-469C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-171C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1969C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu248Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

17-27944531-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944531
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944531
    reference: chr 17
allele count: 1
allele frequency: 8.950628334109055e-6
allele num: 111724
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-471G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.605G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.740G>C
  hgvsp: ENSP00000344562.5:p.Gly247Ala
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56814C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1814G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.740G>C
  hgvsp: ENSP00000373419.3:p.Gly247Ala
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1967G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-471G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-173G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-173G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-471G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-666G>C
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly247Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

17-27944531-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944531
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944531
    reference: chr 17
allele count: 1
allele frequency: 8.950628334109055e-6
allele num: 111724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.740G>A
  hgvsp: ENSP00000373419.3:p.Gly247Asp
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56814C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-471G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1814G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-471G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-471G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.740G>A
  hgvsp: ENSP00000344562.5:p.Gly247Asp
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-173G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.605G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1967G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-666G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-173G>A
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly247Asp
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/17-27944532-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944532
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944532
    reference: chr 17
allele count: 1
allele frequency: 8.965875876414367e-6
allele num: 111534
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-472G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-174G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.739G>T
  hgvsp: ENSP00000373419.3:p.Gly247Cys
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-667G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-472G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-174G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56815C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1966G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.739G>T
  hgvsp: ENSP00000344562.5:p.Gly247Cys
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1813G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.604G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-472G>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8862
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly247Cys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

17-27944541-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944541
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944541
    reference: chr 17
allele count: 1
allele frequency: 9.115936480154606e-6
allele num: 109698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-481C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-481C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1957C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-183C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-183C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-676C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.595C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1804C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.730C>A
  hgvsp: ENST00000388767.3:c.730C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.730C>A
  hgvsp: ENST00000345068.5:c.730C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-481C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56824G>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7870
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg244Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

17-27944543-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944543
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944543
    reference: chr 17
allele count: 2
allele frequency: 1.821427270409093e-5
allele num: 109804
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.728A>G
  hgvsp: ENSP00000373419.3:p.Gln243Arg
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.593A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.728A>G
  hgvsp: ENSP00000344562.5:p.Gln243Arg
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-483A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56826T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-678A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1802A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-185A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1955A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-483A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-185A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-483A>G
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln243Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

17-27944546-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944546
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944546
    reference: chr 17
allele count: 1
allele frequency: 9.188811702870585e-6
allele num: 108828
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56829C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.725G>C
  hgvsp: ENSP00000373419.3:p.Ser242Thr
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1952G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1799G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.725G>C
  hgvsp: ENSP00000344562.5:p.Ser242Thr
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-188G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-188G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-486G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-681G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-486G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.590G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-486G>C
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser242Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

17-27944549-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944549
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944549
    reference: chr 17
allele count: 1
allele frequency: 9.343873222328119e-6
allele num: 107022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1796T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-191T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-489T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.587T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.722T>A
  hgvsp: ENSP00000344562.5:p.Met241Lys
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-489T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-489T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.722T>A
  hgvsp: ENSP00000373419.3:p.Met241Lys
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1949T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-191T>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56832A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-684T>A
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5712
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15121
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met241Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/17-27944552-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944552
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944552
    reference: chr 17
allele count: 1
allele frequency: 9.507872518445273e-6
allele num: 105176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.584G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-492G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.719G>T
  hgvsp: ENSP00000373419.3:p.Arg240Leu
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-492G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-687G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-194G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-492G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1793G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1946G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.719G>T
  hgvsp: ENSP00000344562.5:p.Arg240Leu
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56835C>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-194G>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg240Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

17-27944552-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944552
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944552
    reference: chr 17
allele count: 2
allele frequency: 1.901574503689055e-5
allele num: 105176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.719G>A
  hgvsp: ENSP00000373419.3:p.Arg240His
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-194G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.584G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-687G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.719G>A
  hgvsp: ENSP00000344562.5:p.Arg240His
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-492G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.754-492G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1946G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1793G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.754-492G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-194G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56835C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15081
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23448
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg240His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

17-27944564-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944564
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944564
    reference: chr 17
allele count: 1
allele frequency: 1.003029148027042e-5
allele num: 99698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-504C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.707C>T
  hgvsp: ENSP00000344562.5:p.Thr236Met
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-206C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-206C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1781C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+502C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+502C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-699C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56847G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.707C>T
  hgvsp: ENSP00000373419.3:p.Thr236Met
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.572C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1934C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr236Met
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: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

17-27944569-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944569
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944569
    reference: chr 17
allele count: 2
allele frequency: 2.069921963941959e-5
allele num: 96622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-704C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-509C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.702C>T
  hgvsp: ENST00000388767.3:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1776C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+497C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.567C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-211C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.702C>T
  hgvsp: ENST00000345068.5:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56852G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1929C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+497C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-211C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe234Phe
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

17-27944578-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944578
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944578
    reference: chr 17
allele count: 1
allele frequency: 1.1168691922802e-5
allele num: 89536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-220C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+488C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1920C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.558C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-713C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-518C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-220C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.693C>T
  hgvsp: ENST00000388767.3:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1767C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.693C>T
  hgvsp: ENST00000345068.5:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+488C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56861G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11724
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly231Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

17-27944583-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944583
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944583
    reference: chr 17
allele count: 2
allele frequency: 2.309682187730968e-5
allele num: 86592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-718C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-523C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.688C>T
  hgvsp: ENSP00000344562.5:p.Gln230Ter
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1915C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1762C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.688C>T
  hgvsp: ENSP00000373419.3:p.Gln230Ter
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-225C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+483C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.553C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+483C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56866G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-225C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9857
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln230Ter
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/17-27944585-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944585
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944585
    reference: chr 17
allele count: 2
allele frequency: 2.392344497607656e-5
allele num: 83600
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-227G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.686G>T
  hgvsp: ENSP00000344562.5:p.Arg229Leu
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+481G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1913G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+481G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56868C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.686G>T
  hgvsp: ENSP00000373419.3:p.Arg229Leu
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.551G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1760G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-525G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-227G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-720G>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15625
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8484
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg229Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP

17-27944590-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944590
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944590
    reference: chr 17
allele count: 1
allele frequency: 1.222434110801428e-5
allele num: 81804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.546C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1908C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+476C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-232C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-530C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1755C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+476C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.681C>T
  hgvsp: ENST00000388767.3:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56873G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-725C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-232C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.681C>T
  hgvsp: ENST00000345068.5:c.681C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe227Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

17-27944593-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944593
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944593
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 80100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+473C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.543C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-728C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.678C>T
  hgvsp: ENST00000388767.3:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-235C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+473C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1905C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.678C>T
  hgvsp: ENST00000345068.5:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-533C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56876G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1752C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-235C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17209
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val226Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

17-27944596-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944596
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944596
    reference: chr 17
allele count: 3
allele frequency: 3.943010356973871e-5
allele num: 76084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.675C>T
  hgvsp: ENST00000388767.3:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1749C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-536C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.675C>T
  hgvsp: ENST00000345068.5:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1902C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56879G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+470C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.540C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-238C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+470C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-238C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-731C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9920
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala225Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

17-27944598-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944598
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944598
    reference: chr 17
allele count: 1
allele frequency: 1.318530629466523e-5
allele num: 75842
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-538G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+468G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1747G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56881C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.538G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.673G>A
  hgvsp: ENSP00000344562.5:p.Ala225Thr
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.673G>A
  hgvsp: ENSP00000373419.3:p.Ala225Thr
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-240G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-240G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+468G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-733G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1900G>A
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17563
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10123
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala225Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

17-27944600-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944600
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944600
    reference: chr 17
allele count: 1
allele frequency: 1.326858265000133e-5
allele num: 75366
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.671G>C
  hgvsp: ENSP00000344562.5:p.Arg224Pro
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-242G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.671G>C
  hgvsp: ENSP00000373419.3:p.Arg224Pro
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1898G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+466G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+466G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-242G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-735G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1745G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56883C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-540G>C
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.536G>C
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10209
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18802
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg224Pro
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

17-27944600-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944600
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944600
    reference: chr 17
allele count: 2
allele frequency: 2.653716530000265e-5
allele num: 75366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+466G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56883C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.536G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+466G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-735G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-540G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1898G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1745G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-242G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.671G>A
  hgvsp: ENSP00000344562.5:p.Arg224Gln
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.671G>A
  hgvsp: ENSP00000373419.3:p.Arg224Gln
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-242G>A
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10209
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18802
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg224Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

17-27944601-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944601
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944601
    reference: chr 17
allele count: 1
allele frequency: 1.344736700554031e-5
allele num: 74364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+465C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+465C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.670C>G
  hgvsp: ENSP00000373419.3:p.Arg224Gly
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-541C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1744C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.670C>G
  hgvsp: ENSP00000344562.5:p.Arg224Gly
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-736C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.535C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-243C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-243C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56884G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1897C>G
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17640
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg224Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

17-27944602-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944602
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944602
    reference: chr 17
allele count: 1
allele frequency: 1.360174102285093e-5
allele num: 73520
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+464G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.534G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-244G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+464G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1743G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.669G>A
  hgvsp: ENSP00000344562.5:p.Met223Ile
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.669G>A
  hgvsp: ENSP00000373419.3:p.Met223Ile
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1896G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-737G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-244G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56885C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-542G>A
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17904
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met223Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

17-27944607-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944607
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944607
    reference: chr 17
allele count: 2
allele frequency: 2.777546315584812e-5
allele num: 72006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1738C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-547C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1891C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-249C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+459C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.664C>G
  hgvsp: ENSP00000344562.5:p.Pro222Ala
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.664C>G
  hgvsp: ENSP00000373419.3:p.Pro222Ala
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.529C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+459C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56890G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-742C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-249C>G
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9079
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro222Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

17-27944620-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944620
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944620
    reference: chr 17
allele count: 12
allele frequency: 1.861619609059882e-4
allele num: 64460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1878C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1725C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-262C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.651C>T
  hgvsp: ENST00000388767.3:c.651C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+446C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+446C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-262C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.651C>T
  hgvsp: ENST00000345068.5:c.651C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.516C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-560C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56903G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-755C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18310
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22565
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His217His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

17-27944623-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944623
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944623
    reference: chr 17
allele count: 1
allele frequency: 1.574902356053925e-5
allele num: 63496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-758C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+443C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.648C>T
  hgvsp: ENST00000388767.3:c.648C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-265C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1722C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-563C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.513C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+443C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-265C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.648C>T
  hgvsp: ENST00000345068.5:c.648C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56906G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1875C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18435
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala216Ala
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

17-27944627-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944627
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944627
    reference: chr 17
allele count: 7
allele frequency: 1.182512331914319e-4
allele num: 59196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.644C>T
  hgvsp: ENSP00000373419.3:p.Ala215Val
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56910G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.644C>T
  hgvsp: ENSP00000344562.5:p.Ala215Val
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-269C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+439C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1871C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-269C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1718C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.509C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-762C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-567C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+439C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18600
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6229
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala215Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

17-27944627-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944627
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944627
    reference: chr 17
allele count: 1
allele frequency: 1.689303331306169e-5
allele num: 59196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-269C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1871C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+439C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1718C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-567C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-269C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.644C>G
  hgvsp: ENSP00000344562.5:p.Ala215Gly
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+439C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.644C>G
  hgvsp: ENSP00000373419.3:p.Ala215Gly
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56910G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-762C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.509C>G
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala215Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/17-27944635-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944635
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944635
    reference: chr 17
allele count: 1
allele frequency: 1.737076153418566e-5
allele num: 57568
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-770G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-575G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-277G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.501G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.636G>T
  hgvsp: ENSP00000373419.3:p.Glu212Asp
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.636G>T
  hgvsp: ENSP00000344562.5:p.Glu212Asp
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1710G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-277G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1863G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+431G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+431G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56918C>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu212Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

17-27944639-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944639
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944639
    reference: chr 17
allele count: 1
allele frequency: 1.801996612246369e-5
allele num: 55494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-2A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+427A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-579A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-2A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56922T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.497A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1859A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+427A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-281A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-281A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1706A>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-774A>G
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.634-2A>G
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

17-27944639-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944639
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944638
    reference: chr 17
allele count: 1
allele frequency: 1.801996612246369e-5
allele num: 55494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-580delC
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.496delC
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-3delC
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1858delC
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56928delG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+426delC
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-282delC
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+426delC
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-3delC
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-282delC
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1705delC
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-775delC
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19203
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.634-3delC
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: TG
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

17-27944640-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944640
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944640
    reference: chr 17
allele count: 1
allele frequency: 1.834122005795825e-5
allele num: 54522
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-3C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1705C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+426C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-775C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+426C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-282C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56923G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.496C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-3C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-580C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1858C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-282C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.634-3C>T
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

17-27944640-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944640
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944640
    reference: chr 17
allele count: 1
allele frequency: 1.834122005795825e-5
allele num: 54522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1858C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-282C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-3C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.496C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-3C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+426C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-282C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+426C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56923G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-580C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1705C>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-775C>A
  variant of: http://identifiers.org/hgnc/21356
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.634-3C>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

17-27944647-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944647
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944647
    reference: chr 17
allele count: 1
allele frequency: 1.957406827435014e-5
allele num: 51088
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56930G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-10C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1698C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1851C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.489C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-289C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-782C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-587C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+419C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+419C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-10C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-289C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19042
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-27944660-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944660
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944660
    reference: chr 17
allele count: 1
allele frequency: 2.133378845415369e-5
allele num: 46874
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.476T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56943A>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-23T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+406T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1838T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-795T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1685T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+406T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-23T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-302T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-302T>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-600T>G
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18040
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9872
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-27944663-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944663
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944663
    reference: chr 17
allele count: 1
allele frequency: 2.176278563656148e-5
allele num: 45950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+403C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-26C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-798C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1835C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-305C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-26C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+403C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.473C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1682C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-305C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-603C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56946G>A
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17886
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

17-27944664-A-ACAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944664
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944667
    reference: chr 17
allele count: 1
allele frequency: 2.197898808738846e-5
allele num: 45498
alternate allele: ACAT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1678_1680dupATG
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-607_634-605dupATG
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-30_634-28dupATG
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-309_71-307dupATG
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-30_634-28dupATG
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1831_1833dupATG
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.469_471dupATG
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-802_221-800dupATG
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-309_-48-307dupATG
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+399_753+401dupATG
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56950_153+56952dupTCA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+399_753+401dupATG
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17760
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD

17-27944684-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944684
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944684
    reference: chr 17
allele count: 1
allele frequency: 2.629088232201073e-5
allele num: 38036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-47G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1661G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-819G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+382G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-624G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-47G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-326G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-326G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.452G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1814G>A
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56967C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+382G>A
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28602
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14858
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

17-27944686-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27944686
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27944686
    reference: chr 17
allele count: 1
allele frequency: 2.863852454321553e-5
allele num: 34918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-821C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+380C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.450C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-49C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1659C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-49C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.634-626C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+380C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1812C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+56969G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.71-328C>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-48-328C>T
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29077
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/17-27945017-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27945017
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27945017
    reference: chr 17
allele count: 1
allele frequency: 3.223726627981947e-4
allele num: 3102
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.70+49G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-1152G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-380G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1328G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1481G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.119G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.633+791G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-49+49G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+49G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+49G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-380G>T
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+57300C>A
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

17-27945030-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27945030
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27945030
    reference: chr 17
allele count: 1
allele frequency: 3.006614552014432e-4
allele num: 3326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1315C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.633+778C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1468C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.106C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+57313G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.753+36C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-1165C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.70+36C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-393C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-49+36C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-393C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.753+36C>G
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

17-27945112-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 27945112
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 27945112
    reference: chr 17
allele count: 1
allele frequency: 1.856665428889714e-4
allele num: 5386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000462627
  ensembl transcript: ENST00000584969
  gene symbol: CORO6
  hgvsc: ENST00000584969.1:c.707C>G
  hgvsp: ENSP00000462627.1:p.Thr236Ser
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000463723
  ensembl transcript: ENST00000580212
  gene symbol: CORO6
  hgvsc: ENST00000580212.1:c.633+696C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000577909
  gene symbol: CORO6
  hgvsc: ENST00000577909.1:n.221-1247C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000373419
  ensembl transcript: ENST00000388767
  gene symbol: CORO6
  hgvsc: ENST00000388767.3:c.634-475C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000467534
  gene symbol: CORO6
  hgvsc: ENST00000467534.1:n.1233C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000403019
  ensembl transcript: ENST00000456796
  gene symbol: CORO6
  hgvsc: ENST00000456796.3:c.-95C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000393624
  ensembl transcript: ENST00000445145
  gene symbol: CORO6
  hgvsc: ENST00000445145.2:c.707C>G
  hgvsp: ENSP00000393624.2:p.Thr236Ser
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000464621
  ensembl transcript: ENST00000480954
  gene symbol: CORO6
  hgvsc: ENST00000480954.2:c.24C>G
  hgvsp: ENSP00000464621.1:p.Thr9Ser
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000469090
  gene symbol: CORO6
  hgvsc: ENST00000469090.1:n.24C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000264031
  ensembl transcript: ENST00000581474
  gene symbol: RP11-68I3.2
  hgvsc: ENST00000581474.1:n.153+57395G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167549
  ensembl transcript: ENST00000459686
  gene symbol: CORO6
  hgvsc: ENST00000459686.1:n.1386C>G
  variant of: http://identifiers.org/hgnc/21356
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167549
  ensembl protein: ENSP00000344562
  ensembl transcript: ENST00000345068
  gene symbol: CORO6
  hgvsc: ENST00000345068.5:c.634-475C>G
  variant of: http://identifiers.org/hgnc/21356
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr236Ser
num of homozygotes: 0
reference allele: G

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

GenotypeDepth
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7589
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30735
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3191
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3391
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5432
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.529987760097919e-4
allele num: 6536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.90751e5

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.35e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.051e1

VQSLOD
type: SiteQuality
SIO_000300: -6.139e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.57e-1

MQ
type: SiteQuality
SIO_000300: 5.72e1

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

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

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

GenotypeQuality
all individuals: 299
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30484
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3550
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7631
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2784
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.944012441679627e-4
allele num: 5144
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.468e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.653e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

QD
type: SiteQuality
SIO_000300: 4.88e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.845e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.439999999999999e-2

DP
type: SiteQuality
SIO_000300: 2.8093e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e0

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

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

GenotypeDepth
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31695
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8690
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1474
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.378378378378379e-3
allele num: 296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6010
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.043e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.01e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.389999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

DP
type: SiteQuality
SIO_000300: 2.73719e5

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

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

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

GenotypeQuality
all individuals: 40
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10626
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 32236
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1655
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2682
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1557
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 9.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1276
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5410
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 2.68345e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.073e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.23e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

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

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

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

GenotypeQuality
all individuals: 140
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1926
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 1134
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 3878
num of homozygotes: 0

East 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

South Asian
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allele frequency: 0.0e0
allele num: 4934
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
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allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

QD
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SIO_000300: 1.433e1

FS
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MQ
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DP
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ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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SIO_000300: -6.93e-2

BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 100
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 4.409171075837742e-4
allele num: 4536
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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.658160552897395e-4
allele num: 3762
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 5.08e-2

BaseQRankSum
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MQRankSum
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SIO_000300: 3.58e-1

FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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QD
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DP
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SIO_000300: 2.81137e5

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.269632319564231e-4
allele num: 4406
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Other
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 1.915708812260536e-3
allele num: 1044
num of homozygotes: 0

Latino
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allele frequency: 3.355704697986577e-3
allele num: 298
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3690
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 82
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 320
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African
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allele count: 0
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InbreedingCoeff
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SIO_000300: -6.26e-2

VQSLOD
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MQ
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SIO_000300: 6.0e1

FS
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DP
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QD
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GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 422
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3830
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1008
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.54841997961264e-4
allele num: 3924
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
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BaseQRankSum
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SIO_000300: 7.36e-1

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1072
num of homozygotes: 0

Other
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Latino
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African
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European (Non-Finnish)
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allele num: 9544
num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 6.91085003455425e-4
allele num: 2894
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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DP
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FS
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QD
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 2888
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European (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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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 4.854840275754928e-5
allele num: 20598
num of homozygotes: 0

MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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QD
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DP
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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East Asian
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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 frequency: 7.139287499107589e-5
allele num: 28014
num of homozygotes: 0

Other
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South Asian
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MQRankSum
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SIO_000300: 3.8e-1

InbreedingCoeff
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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BaseQRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 4492
num of homozygotes: 0

South Asian
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allele frequency: 1.675603217158177e-4
allele num: 5968
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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Latino
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MQRankSum
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 1.617599482368166e-4
allele num: 6182
num of homozygotes: 0

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

East Asian
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Latino
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Other
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European (Finnish)
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allele frequency: 0.0e0
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African
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ClippingRankSum
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SIO_000300: 9.2e-2

InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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ReadPosRankSum
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MQ
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.641658731982795e-5
allele num: 60914
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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African
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

DP
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MQ
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
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allele num: 60882
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Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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num of homozygotes: 0

South Asian
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MQ
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BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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Latino
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ClippingRankSum
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VQSLOD
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FS
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DP
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MQ
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MQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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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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BaseQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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QD
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FS
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MQRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele count: 1
allele frequency: 1.269035532994924e-3
allele num: 788
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6208
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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61022
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MQ
type: SiteQuality
SIO_000300: 5.935e1

InbreedingCoeff
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DP
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QD
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FS
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SIO_000300: 3.328e0

BaseQRankSum
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ReadPosRankSum
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SIO_000300: -8.139999999999999e-1

MQRankSum
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VQSLOD
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SIO_000300: 2.92e-1

ClippingRankSum
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SIO_000300: 1.02e0

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: 4.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6166
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

European (Non-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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allele num: 8364
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VQSLOD
type: SiteQuality
SIO_000300: -9.322e-1

MQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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MQ
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ReadPosRankSum
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FS
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SIO_000300: 7.256e0

BaseQRankSum
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DP
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SIO_000300: 1.464971e6

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13728
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61286
num of homozygotes: 0

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

African
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allele frequency: 1.153668666359022e-4
allele num: 8668
num of homozygotes: 0

Other
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num of homozygotes: 0

VQSLOD
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SIO_000300: 1.38e0

FS
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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DP
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QD
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SIO_000300: 1.05e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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
all individuals: 115
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.153668666359022e-4
allele num: 8668
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61298
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
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FS
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SIO_000300: 1.379e0

InbreedingCoeff
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MQRankSum
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ClippingRankSum
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VQSLOD
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DP
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MQ
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SIO_000300: 5.972e1

ReadPosRankSum
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SIO_000300: -3.82e-1

BaseQRankSum
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QD
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SIO_000300: 1.021e1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 30

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8678
num of homozygotes: 0

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

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

South Asian
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allele count: 29
allele frequency: 1.942658092175777e-3
allele num: 14928
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61628
num of homozygotes: 0

Latino
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allele frequency: 8.852691218130312e-5
allele num: 11296
num of homozygotes: 0

European (Finnish)
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ClippingRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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MQRankSum
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8678
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.622639060167456e-5
allele num: 61628
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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num of homozygotes: 0

East 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
allele num: 11296
num of homozygotes: 0

European (Finnish)
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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FS
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DP
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MQ
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.25e1
variant carriers: 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
allele num: 15014
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele frequency: 1.783340358613534e-4
allele num: 61682
num of homozygotes: 0

Other
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ClippingRankSum
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DP
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1463
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.16333178222429e-4
allele num: 8596
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11288
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

QD
type: SiteQuality
SIO_000300: 9.359999999999999e0

DP
type: SiteQuality
SIO_000300: 1.484715e6

FS
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 2.78e0

BaseQRankSum
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SIO_000300: -2.495e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

GenotypeDepth
all individuals: 661
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1267
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 94
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variant carriers: 1

GenotypeQuality
all individuals: 42131
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.627975124540097e-5
allele num: 61426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

BaseQRankSum
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SIO_000300: -8.400000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.031e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

DP
type: SiteQuality
SIO_000300: 1.479732e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.98e-1

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

GenotypeQuality
all individuals: 293
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1446
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.692620176032498e-4
allele num: 5908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15444
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

FS
type: SiteQuality
SIO_000300: 1.031e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.479732e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 6
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 243
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5868
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61322
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.198753296571566e-4
allele num: 8342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15466
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 9.96e-1

QD
type: SiteQuality
SIO_000300: 2.345e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.678e0

DP
type: SiteQuality
SIO_000300: 1.474463e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.054e0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 85
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variant carriers: 1

GenotypeQuality
all individuals: 987
bin: 7.5e0
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.659971448491086e-5
allele num: 60242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15542
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11048
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.886e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

DP
type: SiteQuality
SIO_000300: 1.42888e6

QD
type: SiteQuality
SIO_000300: 1.453e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.712e-1

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5626
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.281394156842645e-4
allele num: 15608
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e0

DP
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 2.07e-1

FS
type: SiteQuality
SIO_000300: 8.25e-1

InbreedingCoeff
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SIO_000300: -2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e-1

QD
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SIO_000300: 1.17e1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 368
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.237623762376238e-4
allele num: 8080
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59748
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8178
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5520
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

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

VQSLOD
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FS
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DP
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InbreedingCoeff
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SIO_000300: -2.9e-3

QD
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -1.934e0

ReadPosRankSum
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SIO_000300: 2.48e-1

MQ
type: SiteQuality
SIO_000300: 5.886e1

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
all individuals: 76
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variant carriers: 1

GenotypeQuality
all individuals: 1090
bin: 2.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15396
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.248439450686642e-4
allele num: 8010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58782
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5374
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.25e-1

DP
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SIO_000300: 1.365883e6

MQRankSum
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MQ
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FS
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -9.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 140
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10506
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.729385722191477e-5
allele num: 57824
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: 7766
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5224
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.335024e6

MQRankSum
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SIO_000300: -3.4e-2

ClippingRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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SIO_000300: 4.23e-1

BaseQRankSum
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SIO_000300: -5.2e-1

QD
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SIO_000300: 7.09e0

VQSLOD
type: SiteQuality
SIO_000300: -5.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5224
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10506
num of homozygotes: 0

African
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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 frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.56254101588135e-5
allele num: 15238
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.729385722191477e-5
allele num: 57824
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

QD
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SIO_000300: 7.09e0

MQRankSum
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SIO_000300: -3.4e-2

InbreedingCoeff
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BaseQRankSum
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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SIO_000300: -4.24e-1

MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 1.335024e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54916
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.372495196266813e-4
allele num: 7286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4858
num of homozygotes: 0

Latino
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: 720
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

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.52e-1

InbreedingCoeff
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SIO_000300: -4.1e-3

FS
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SIO_000300: 1.394e0

BaseQRankSum
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SIO_000300: -3.19e-1

ClippingRankSum
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SIO_000300: -1.099e0

DP
type: SiteQuality
SIO_000300: 1.20102e6

QD
type: SiteQuality
SIO_000300: 7.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

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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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4660
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7030
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 53150
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.374003847210772e-4
allele num: 14556
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9358
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.76e-1

VQSLOD
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DP
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SIO_000300: 1.140642e6

QD
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -4.9e-3

FS
type: SiteQuality
SIO_000300: 6.81e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 1.19e0

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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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
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)
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.035581972886048e-5
allele num: 49126
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

Latino
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.511e0

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

African
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allele count: 1
allele frequency: 1.548946716232962e-4
allele num: 6456
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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47480
num of homozygotes: 0

Latino
type: Population
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allele num: 7990
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Other
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East Asian
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European (Finnish)
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.369292611526194e-5
allele num: 45774
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
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South Asian
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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European (Finnish)
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Other
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African
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European (Non-Finnish)
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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QD
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DP
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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African
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Latino
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Other
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European (Non-Finnish)
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DP
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MQ
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Other
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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 frequency: 4.805382027871216e-5
allele num: 41620
num of homozygotes: 0

European (Finnish)
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Latino
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allele num: 6658
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FS
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MQ
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VQSLOD
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QD
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DP
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 1.517450682852807e-4
allele num: 6590
num of homozygotes: 0

European (Finnish)
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East Asian
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African
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South Asian
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European (Non-Finnish)
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Other
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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DP
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MQ
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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allele num: 41240
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Latino
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Other
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South Asian
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European (Finnish)
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ClippingRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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South Asian
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Latino
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ReadPosRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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VQSLOD
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FS
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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African
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Other
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European (Finnish)
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MQRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: 2.12e-1

DP
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SIO_000300: 8.18709e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 40262
num of homozygotes: 0

South Asian
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allele frequency: 7.925186241876684e-5
allele num: 12618
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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East 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

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

MQRankSum
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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SIO_000300: 6.0e1

DP
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ClippingRankSum
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SIO_000300: -1.1e-2

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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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 39412
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

African
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allele frequency: 3.795066413662239e-4
allele num: 5270
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
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VQSLOD
type: SiteQuality
SIO_000300: -1.511e-1

ReadPosRankSum
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DP
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FS
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SIO_000300: 6.791e0

ClippingRankSum
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SIO_000300: 9.9e-2

MQRankSum
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -1.01e-2

BaseQRankSum
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SIO_000300: 1.42e0

QD
type: SiteQuality
SIO_000300: 1.122e1

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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2692
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.892505677517033e-4
allele num: 5284
num of homozygotes: 0

Other
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East Asian
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allele count: 0
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African
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allele frequency: 4.286326618088298e-4
allele num: 4666
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 9
allele frequency: 2.552756977535738e-4
allele num: 35256
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DP
type: SiteQuality
SIO_000300: 7.14316e5

VQSLOD
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QD
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ClippingRankSum
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FS
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InbreedingCoeff
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SIO_000300: -1.31e-2

ReadPosRankSum
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SIO_000300: -4.4e-2

MQRankSum
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SIO_000300: 4.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -8.129999999999999e-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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4600
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.879189220315559e-5
allele num: 34732
num of homozygotes: 0

Latino
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Other
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European (Finnish)
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MQRankSum
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SIO_000300: 2.15e0

ReadPosRankSum
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DP
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InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Finnish)
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allele frequency: 0.0e0
allele num: 2366
num of homozygotes: 0

African
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allele frequency: 2.327746741154562e-4
allele num: 4296
num of homozygotes: 0

East Asian
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allele num: 4180
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 1.23296960729918e-4
allele num: 32442
num of homozygotes: 0

South Asian
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allele frequency: 9.203018590097552e-5
allele num: 10866
num of homozygotes: 0

Latino
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Other
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QD
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 3.08242401824795e-5
allele num: 32442
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2226
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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num of homozygotes: 0

South Asian
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Latino
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Other
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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FS
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ReadPosRankSum
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VQSLOD
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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bin: 8.75e1
variant carriers: 0

African
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allele frequency: 2.44140625e-4
allele num: 4096
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4230
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 30442
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 4058
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10158
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

DP
type: SiteQuality
SIO_000300: 6.31856e5

VQSLOD
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.66e-2

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: -2.59e-1

QD
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GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4230
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2136
num of homozygotes: 0

African
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allele count: 1
allele frequency: 2.44140625e-4
allele num: 4096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30442
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 374
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 frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQ
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FS
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DP
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MQRankSum
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ClippingRankSum
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VQSLOD
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QD
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SIO_000300: 5.28e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3998
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 29934
num of homozygotes: 0

South Asian
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num of homozygotes: 0

East Asian
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VQSLOD
type: SiteQuality
SIO_000300: 8.4e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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ClippingRankSum
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MQ
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DP
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 1.26e0

QD
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SIO_000300: 1.02e1

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.340682835571591e-5
allele num: 29934
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4120
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3998
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

BaseQRankSum
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SIO_000300: -2.293e0

FS
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 8.4e-1

ClippingRankSum
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SIO_000300: -9.88e-1

QD
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ReadPosRankSum
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MQRankSum
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SIO_000300: -6.66e-1

InbreedingCoeff
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SIO_000300: 1.69e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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SIO_000300: 6.21087e5

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
all individuals: 32
bin: 8.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3758
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

African
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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: 3736
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.057753331922996e-4
allele num: 9454
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 28166
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
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SIO_000300: -2.783e0

MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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MQ
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QD
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.076e0

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: 5.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3282
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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3464
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.860407659048796e-5
allele num: 25904
num of homozygotes: 0

Other
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South Asian
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East Asian
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VQSLOD
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BaseQRankSum
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FS
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MQ
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QD
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8612
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

East Asian
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Other
type: Population
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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 num: 25424
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MQ
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DP
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QD
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 244
bin: 4.75e1
variant carriers: 0

East Asian
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allele count: 1
allele frequency: 2.979737783075089e-4
allele num: 3356
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25176
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
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SIO_000300: -2.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 5.3764e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.17e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.4e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 3803
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.718761796904492e-5
allele num: 21192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2912
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2450
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1260
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7040
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 5.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: -4.37e-1

BaseQRankSum
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SIO_000300: -1.537e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.91e-2

QD
type: SiteQuality
SIO_000300: 1.473e1

DP
type: SiteQuality
SIO_000300: 4.96939e5

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 8
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2742
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.63821892393321e-4
allele num: 2156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.08e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.76e0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
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SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.94443e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.144e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 91
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1895
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 5.213764337851929e-4
allele num: 1918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
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
allele num: 30
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 166
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.0649e4

ClippingRankSum
type: SiteQuality
SIO_000300: 8.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.96e-2

QD
type: SiteQuality
SIO_000300: 1.058e1

VQSLOD
type: SiteQuality
SIO_000300: -1.506e0

FS
type: SiteQuality
SIO_000300: 5.825e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -2.054e0

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 408
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 9.259259259259259e-3
allele num: 108
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2070
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.31e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.398e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 4.62e-1

QD
type: SiteQuality
SIO_000300: 9.66e0

DP
type: SiteQuality
SIO_000300: 5.3603e4

BaseQRankSum
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SIO_000300: 9.54e-1

FS
type: SiteQuality
SIO_000300: 4.304e0

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2