11-65623543-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623543
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623543
    reference: chr 11
allele count: 394
allele frequency: 3.245148749711725e-3
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.174C>T
  hgvsp: ENST00000308162.5:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.174C>T
  hgvsp: ENST00000526975.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.174C>T
  hgvsp: ENST00000532134.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.269C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.123C>T
  hgvsp: ENST00000534784.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.174C>T
  hgvsp: ENST00000525451.2:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.123C>T
  hgvsp: ENST00000524553.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.123C>T
  hgvsp: ENST00000531407.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+2025C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.123C>T
  hgvsp: ENST00000530413.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.288C>T
  hgvsp: ENST00000534769.1:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.123C>T
  hgvsp: ENST00000531413.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1649-57G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.123C>T
  hgvsp: ENST00000527344.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2755
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly58Gly
num of homozygotes: 8
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

11-65623548-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623548
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623548
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.169G>C
  hgvsp: ENSP00000432153.1:p.Val57Leu
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1649-52C>G
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.169G>C
  hgvsp: ENSP00000432660.1:p.Val57Leu
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+2020G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.118G>C
  hgvsp: ENSP00000436899.1:p.Val40Leu
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.169G>C
  hgvsp: ENSP00000436431.1:p.Val57Leu
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.118G>C
  hgvsp: ENSP00000433131.1:p.Val40Leu
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.118G>C
  hgvsp: ENSP00000433308.1:p.Val40Leu
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.118G>C
  hgvsp: ENSP00000432226.1:p.Val40Leu
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.169G>C
  hgvsp: ENSP00000309629.5:p.Val57Leu
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.264G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.118G>C
  hgvsp: ENSP00000432155.1:p.Val40Leu
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.283G>C
  hgvsp: ENSP00000431696.1:p.Val95Leu
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.118G>C
  hgvsp: ENSP00000433910.1:p.Val40Leu
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10979
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val57Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD

11-65623549-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623549
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623549
    reference: chr 11
allele count: 9
allele frequency: 7.412898443291327e-5
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.117G>C
  hgvsp: ENST00000531407.1:c.117G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.117G>C
  hgvsp: ENST00000534784.1:c.117G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.168G>C
  hgvsp: ENST00000526975.1:c.168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.117G>C
  hgvsp: ENST00000531413.1:c.117G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1649-51C>G
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+2019G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.168G>C
  hgvsp: ENST00000532134.1:c.168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.117G>C
  hgvsp: ENST00000524553.1:c.117G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.263G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.168G>C
  hgvsp: ENST00000525451.2:c.168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.117G>C
  hgvsp: ENST00000530413.1:c.117G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.282G>C
  hgvsp: ENST00000534769.1:c.282G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.168G>C
  hgvsp: ENST00000308162.5:c.168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.117G>C
  hgvsp: ENST00000527344.1:c.117G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu56Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

11-65623552-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623552
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623552
    reference: chr 11
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1649-48G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.165C>T
  hgvsp: ENST00000308162.5:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.165C>T
  hgvsp: ENST00000526975.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.114C>T
  hgvsp: ENST00000534784.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.114C>T
  hgvsp: ENST00000527344.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.165C>T
  hgvsp: ENST00000532134.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.165C>T
  hgvsp: ENST00000525451.2:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.260C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.114C>T
  hgvsp: ENST00000524553.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.114C>T
  hgvsp: ENST00000531407.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.279C>T
  hgvsp: ENST00000534769.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.114C>T
  hgvsp: ENST00000531413.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+2016C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.114C>T
  hgvsp: ENST00000530413.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile55Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-65623567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623567
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623567
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.150G>A
  hgvsp: ENST00000308162.5:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.150G>A
  hgvsp: ENST00000526975.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.150G>A
  hgvsp: ENST00000525451.2:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.99G>A
  hgvsp: ENST00000531407.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+2001G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.150G>A
  hgvsp: ENST00000532134.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.99G>A
  hgvsp: ENST00000524553.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1649-33C>T
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.99G>A
  hgvsp: ENST00000534784.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.99G>A
  hgvsp: ENST00000527344.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.99G>A
  hgvsp: ENST00000531413.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.264G>A
  hgvsp: ENST00000534769.1:c.264G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.99G>A
  hgvsp: ENST00000530413.1:c.99G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.245G>A
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu50Glu
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/11-65623570-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623570
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623570
    reference: chr 11
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.96G>T
  hgvsp: ENST00000524553.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.96G>T
  hgvsp: ENST00000527344.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.147G>T
  hgvsp: ENST00000532134.1:c.147G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.261G>T
  hgvsp: ENST00000534769.1:c.261G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.96G>T
  hgvsp: ENST00000530413.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.96G>T
  hgvsp: ENST00000531407.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.96G>T
  hgvsp: ENST00000531413.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.147G>T
  hgvsp: ENST00000525451.2:c.147G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.147G>T
  hgvsp: ENST00000308162.5:c.147G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.242G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.147G>T
  hgvsp: ENST00000526975.1:c.147G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.96G>T
  hgvsp: ENST00000534784.1:c.96G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1998G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1649-30C>A
  variant of: http://identifiers.org/hgnc/26423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu49Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-65623572-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623572
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623572
    reference: chr 11
allele count: 12
allele frequency: 9.884027411702688e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.94C>T
  hgvsp: ENST00000527344.1:c.94C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1649-28G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.94C>T
  hgvsp: ENST00000531413.1:c.94C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.94C>T
  hgvsp: ENST00000524553.1:c.94C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.94C>T
  hgvsp: ENST00000531407.1:c.94C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.94C>T
  hgvsp: ENST00000534784.1:c.94C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.145C>T
  hgvsp: ENST00000532134.1:c.145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.145C>T
  hgvsp: ENST00000308162.5:c.145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.94C>T
  hgvsp: ENST00000530413.1:c.94C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.145C>T
  hgvsp: ENST00000526975.1:c.145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.259C>T
  hgvsp: ENST00000534769.1:c.259C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.145C>T
  hgvsp: ENST00000525451.2:c.145C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1996C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.240C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11321
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu49Leu
num of homozygotes: 1
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

11-65623572-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623572
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623572
    reference: chr 11
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1996C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.145C>G
  hgvsp: ENSP00000432153.1:p.Leu49Val
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.94C>G
  hgvsp: ENSP00000436899.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.145C>G
  hgvsp: ENSP00000436431.1:p.Leu49Val
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.240C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.94C>G
  hgvsp: ENSP00000433131.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.94C>G
  hgvsp: ENSP00000432226.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.94C>G
  hgvsp: ENSP00000432155.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.145C>G
  hgvsp: ENSP00000432660.1:p.Leu49Val
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.259C>G
  hgvsp: ENSP00000431696.1:p.Leu87Val
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.94C>G
  hgvsp: ENSP00000433910.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.94C>G
  hgvsp: ENSP00000433308.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.145C>G
  hgvsp: ENSP00000309629.5:p.Leu49Val
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1649-28G>C
  variant of: http://identifiers.org/hgnc/26423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu49Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

11-65623573-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623573
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623573
    reference: chr 11
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.93C>T
  hgvsp: ENST00000524553.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.93C>T
  hgvsp: ENST00000527344.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.93C>T
  hgvsp: ENST00000531413.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.144C>T
  hgvsp: ENST00000525451.2:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1649-27G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.258C>T
  hgvsp: ENST00000534769.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.144C>T
  hgvsp: ENST00000532134.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.93C>T
  hgvsp: ENST00000534784.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1995C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.93C>T
  hgvsp: ENST00000531407.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.93C>T
  hgvsp: ENST00000530413.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.239C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.144C>T
  hgvsp: ENST00000526975.1:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.144C>T
  hgvsp: ENST00000308162.5:c.144C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile48Ile
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

11-65623585-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623585
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623585
    reference: chr 11
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.81G>A
  hgvsp: ENST00000527344.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1983G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.81G>A
  hgvsp: ENST00000531407.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.132G>A
  hgvsp: ENST00000308162.5:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.227G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.81G>A
  hgvsp: ENST00000530413.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.81G>A
  hgvsp: ENST00000524553.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.246G>A
  hgvsp: ENST00000534769.1:c.246G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.81G>A
  hgvsp: ENST00000531413.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.132G>A
  hgvsp: ENST00000525451.2:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1649-15C>T
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.132G>A
  hgvsp: ENST00000526975.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.81G>A
  hgvsp: ENST00000534784.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.132G>A
  hgvsp: ENST00000532134.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys44Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

11-65623603-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623603
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623603
    reference: chr 11
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.63C>T
  hgvsp: ENST00000530413.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.63C>T
  hgvsp: ENST00000531407.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1965C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.63C>T
  hgvsp: ENST00000531413.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.63C>T
  hgvsp: ENST00000524553.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.114C>T
  hgvsp: ENST00000532134.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1652G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.63C>T
  hgvsp: ENST00000527344.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.63C>T
  hgvsp: ENST00000534784.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.114C>T
  hgvsp: ENST00000525451.2:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.114C>T
  hgvsp: ENST00000308162.5:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.228C>T
  hgvsp: ENST00000534769.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.114C>T
  hgvsp: ENST00000526975.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.209C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe38Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-65623612-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623612
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623612
    reference: chr 11
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1956G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.105G>T
  hgvsp: ENST00000308162.5:c.105G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.54G>T
  hgvsp: ENST00000531407.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.54G>T
  hgvsp: ENST00000534784.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.200G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.54G>T
  hgvsp: ENST00000524553.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.105G>T
  hgvsp: ENST00000525451.2:c.105G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.219G>T
  hgvsp: ENST00000534769.1:c.219G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.54G>T
  hgvsp: ENST00000530413.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.54G>T
  hgvsp: ENST00000531413.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.105G>T
  hgvsp: ENST00000526975.1:c.105G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.105G>T
  hgvsp: ENST00000532134.1:c.105G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1661C>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.54G>T
  hgvsp: ENST00000527344.1:c.54G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala35Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum

11-65623612-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623612
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623612
    reference: chr 11
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.105G>A
  hgvsp: ENST00000308162.5:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.200G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1956G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.54G>A
  hgvsp: ENST00000534784.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.219G>A
  hgvsp: ENST00000534769.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.54G>A
  hgvsp: ENST00000524553.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.54G>A
  hgvsp: ENST00000531413.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.54G>A
  hgvsp: ENST00000531407.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.105G>A
  hgvsp: ENST00000525451.2:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.105G>A
  hgvsp: ENST00000532134.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.54G>A
  hgvsp: ENST00000530413.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1661C>T
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.54G>A
  hgvsp: ENST00000527344.1:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.105G>A
  hgvsp: ENST00000526975.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala35Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-65623639-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623639
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623639
    reference: chr 11
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.78A>T
  hgvsp: ENST00000525451.2:c.78A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.27A>T
  hgvsp: ENST00000530413.1:c.27A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.78A>T
  hgvsp: ENST00000308162.5:c.78A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.27A>T
  hgvsp: ENST00000534784.1:c.27A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.27A>T
  hgvsp: ENST00000527344.1:c.27A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1688T>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.27A>T
  hgvsp: ENST00000531413.1:c.27A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.27A>T
  hgvsp: ENST00000524553.1:c.27A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.27A>T
  hgvsp: ENST00000531407.1:c.27A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.173A>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.192A>T
  hgvsp: ENST00000534769.1:c.192A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.78A>T
  hgvsp: ENST00000526975.1:c.78A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1929A>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.78A>T
  hgvsp: ENST00000532134.1:c.78A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro26Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

11-65623639-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623639
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623639
    reference: chr 11
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1688T>G
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.27A>C
  hgvsp: ENST00000527344.1:c.27A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.27A>C
  hgvsp: ENST00000530413.1:c.27A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.27A>C
  hgvsp: ENST00000534784.1:c.27A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.78A>C
  hgvsp: ENST00000525451.2:c.78A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.78A>C
  hgvsp: ENST00000532134.1:c.78A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1929A>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.27A>C
  hgvsp: ENST00000531407.1:c.27A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.27A>C
  hgvsp: ENST00000531413.1:c.27A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.78A>C
  hgvsp: ENST00000526975.1:c.78A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.78A>C
  hgvsp: ENST00000308162.5:c.78A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.27A>C
  hgvsp: ENST00000524553.1:c.27A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.173A>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.192A>C
  hgvsp: ENST00000534769.1:c.192A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro26Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

11-65623642-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623642
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623642
    reference: chr 11
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.75G>A
  hgvsp: ENST00000526975.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.75G>A
  hgvsp: ENST00000308162.5:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.170G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.24G>A
  hgvsp: ENST00000524553.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.24G>A
  hgvsp: ENST00000531413.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.24G>A
  hgvsp: ENST00000531407.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1926G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.189G>A
  hgvsp: ENST00000534769.1:c.189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.24G>A
  hgvsp: ENST00000527344.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.24G>A
  hgvsp: ENST00000534784.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.75G>A
  hgvsp: ENST00000532134.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.75G>A
  hgvsp: ENST00000525451.2:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1691C>T
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.24G>A
  hgvsp: ENST00000530413.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr25Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-65623654-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623654
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623654
    reference: chr 11
allele count: 4
allele frequency: 3.295761650517435e-5
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.12T>G
  hgvsp: ENST00000530413.1:c.12T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.12T>G
  hgvsp: ENST00000524553.1:c.12T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.63T>G
  hgvsp: ENST00000532134.1:c.63T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.63T>G
  hgvsp: ENST00000525451.2:c.63T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.12T>G
  hgvsp: ENST00000531413.1:c.12T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.158T>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.12T>G
  hgvsp: ENST00000531407.1:c.12T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.177T>G
  hgvsp: ENST00000534769.1:c.177T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.12T>G
  hgvsp: ENST00000534784.1:c.12T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.63T>G
  hgvsp: ENST00000308162.5:c.63T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.12T>G
  hgvsp: ENST00000527344.1:c.12T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1703A>C
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.63T>G
  hgvsp: ENST00000526975.1:c.63T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1914T>G
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg21Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

11-65623669-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623669
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623669
    reference: chr 11
allele count: 2
allele frequency: 1.648559982854976e-5
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1718G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1899C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.48C>T
  hgvsp: ENST00000532134.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.48C>T
  hgvsp: ENST00000526975.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.48C>T
  hgvsp: ENST00000525451.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.48C>T
  hgvsp: ENST00000308162.5:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.143C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.162C>T
  hgvsp: ENST00000534769.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn16Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

11-65623676-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623676
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623676
    reference: chr 11
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.41T>C
  hgvsp: ENSP00000436431.1:p.Val14Ala
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.41T>C
  hgvsp: ENSP00000309629.5:p.Val14Ala
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.41T>C
  hgvsp: ENSP00000432153.1:p.Val14Ala
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.155T>C
  hgvsp: ENSP00000431696.1:p.Val52Ala
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-11T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-11T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-11T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.41T>C
  hgvsp: ENSP00000432660.1:p.Val14Ala
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-11T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1725A>G
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1892T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.136T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-11T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-11T>C
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val14Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

11-65623693-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623693
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623693
    reference: chr 11
allele count: 1
allele frequency: 8.276090374906894e-6
allele num: 120830
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-28T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-28T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-28T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-28T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1875T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.138T>C
  hgvsp: ENST00000534769.1:c.138T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.24T>C
  hgvsp: ENST00000525451.2:c.24T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-28T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-28T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.24T>C
  hgvsp: ENST00000526975.1:c.24T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1742A>G
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.24T>C
  hgvsp: ENST00000532134.1:c.24T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.119T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.24T>C
  hgvsp: ENST00000308162.5:c.24T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser8Ser
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

11-65623696-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623696
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623696
    reference: chr 11
allele count: 2
allele frequency: 1.656397005234214e-5
allele num: 120744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.21C>T
  hgvsp: ENST00000526975.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.116C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.21C>T
  hgvsp: ENST00000525451.2:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1872C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.21C>T
  hgvsp: ENST00000308162.5:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.135C>T
  hgvsp: ENST00000534769.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-31C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1745G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.21C>T
  hgvsp: ENST00000532134.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7727
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val7Val
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

11-65623708-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623708
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623708
    reference: chr 11
allele count: 33
allele frequency: 2.75027502750275e-4
allele num: 119988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.9C>T
  hgvsp: ENST00000525451.2:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.9C>T
  hgvsp: ENST00000532134.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1860C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.9C>T
  hgvsp: ENST00000526975.1:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.123C>T
  hgvsp: ENST00000534769.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.9C>T
  hgvsp: ENST00000308162.5:c.9C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.104C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1757G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9972
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6273
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser3Ser
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

11-65623711-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623711
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623711
    reference: chr 11
allele count: 3
allele frequency: 2.499541750679042e-5
allele num: 120022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-46C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-46C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.101C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-46C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-46C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.6C>T
  hgvsp: ENST00000308162.5:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.120C>T
  hgvsp: ENST00000534769.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.6C>T
  hgvsp: ENST00000525451.2:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-46C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.6C>T
  hgvsp: ENST00000532134.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1760G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1857C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.6C>T
  hgvsp: ENST00000526975.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-46C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.6C>T
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

11-65623717-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623717
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623717
    reference: chr 11
allele count: 1
allele frequency: 8.354637659364713e-6
allele num: 119694
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1766G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1851C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-52C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-4C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-4C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9935
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.4-4C>T
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

11-65623720-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623720
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623720
    reference: chr 11
allele count: 4
allele frequency: 3.350027637728011e-5
allele num: 119402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-7C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1769G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-7C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-7C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-7C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-7C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-7C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-7C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-7C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-7C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-55C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-7C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-7C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1848C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.4-7C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

11-65623724-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623724
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623724
    reference: chr 11
allele count: 2
allele frequency: 1.678443746957821e-5
allele num: 119158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-11A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-11A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-11A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1773T>C
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-11A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-59A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-11A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-11A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-11A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-11A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1844A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-11A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-11A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-11A>G
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7600
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

11-65623725-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623725
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623725
    reference: chr 11
allele count: 1
allele frequency: 8.399549784131571e-6
allele num: 119054
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-12C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1774G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-12C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-12C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-60C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-12C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1843C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-12C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-12C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-12C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-12C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-12C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-12C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-12C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

11-65623730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623730
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623730
    reference: chr 11
allele count: 2
allele frequency: 1.688590196045322e-5
allele num: 118442
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-17C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1838C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-17C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-65C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-17C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1779G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-17C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-17C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-17C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-17C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-17C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-17C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-17C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-17C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

11-65623734-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623734
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623734
    reference: chr 11
allele count: 7
allele frequency: 5.924371170317208e-5
allele num: 118156
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-69T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-21T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1834T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-21T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-21T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-21T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1783A>G
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-21T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-21T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-21T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-21T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-21T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-21T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-21T>C
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8292
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum

11-65623735-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623735
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623735
    reference: chr 11
allele count: 4
allele frequency: 3.390117806593779e-5
allele num: 117990
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-22G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-22G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-22G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1833G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-22G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-70G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-22G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-22G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-22G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-22G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-22G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1784C>T
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-22G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-22G>A
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

11-65623739-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623739
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623739
    reference: chr 11
allele count: 17677
allele frequency: 1.501333423926891e-1
allele num: 117742
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-26T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1788A>G
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-26T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-26T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-26T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-26T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-26T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-74T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-26T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-26T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-26T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-26T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1829T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-26T>C
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 2.25e1
  variant carriers: 518
genotype depth: GenotypeDepth
  all individuals: 6291
  bin: 4.25e1
  variant carriers: 1185
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.75e1
  variant carriers: 735
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 1.25e1
  variant carriers: 485
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 1.75e1
  variant carriers: 646
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 6.75e1
  variant carriers: 1255
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 5.25e1
  variant carriers: 1692
genotype depth: GenotypeDepth
  all individuals: 7530
  bin: 3.75e1
  variant carriers: 759
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 8014
  bin: 2.75e1
  variant carriers: 430
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 4.75e1
  variant carriers: 1459
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 3.25e1
  variant carriers: 549
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 5.75e1
  variant carriers: 1741
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.25e1
  variant carriers: 253
genotype quality: GenotypeQuality
num of homozygotes: 1540
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

11-65623741-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623741
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623741
    reference: chr 11
allele count: 48
allele frequency: 4.103335669955034e-4
allele num: 116978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-28C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1790G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-76C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-28C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1827C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-28C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-28C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-28C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-28C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-28C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-28C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-28C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-28C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-28C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9287
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11655
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

11-65623742-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623742
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623742
    reference: chr 11
allele count: 6
allele frequency: 5.133821616811555e-5
allele num: 116872
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-29T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1826T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-29T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-29T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-29T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-29T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1791A>G
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-29T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-29T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-77T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-29T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-29T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-29T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-29T>C
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9277
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

11-65623743-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623743
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623743
    reference: chr 11
allele count: 1
allele frequency: 8.567071603584462e-6
allele num: 116726
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-30T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-30T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-78T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1792A>G
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-30T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-30T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-30T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-30T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-30T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-30T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-30T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-30T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-30T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1825T>C
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7022
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

11-65623746-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623746
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623746
    reference: chr 11
allele count: 1
allele frequency: 8.614006374364718e-6
allele num: 116090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-33C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-33C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-81C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-33C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-33C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1795G>T
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-33C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-33C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-33C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-33C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-33C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-33C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-33C>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1822C>A
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

11-65623747-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623747
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623747
    reference: chr 11
allele count: 1
allele frequency: 8.609853115905842e-6
allele num: 116146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-34C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-34C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-34C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-82C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-34C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-34C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1796G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-34C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-34C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-34C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-34C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1821C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-34C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-34C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

11-65623754-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623754
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623754
    reference: chr 11
allele count: 1
allele frequency: 8.680254157841742e-6
allele num: 115204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-41C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-41C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-41C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-41C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1814C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-41C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-41C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-41C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-41C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-41C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-89C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1803G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-41C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-41C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

11-65623755-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623755
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623755
    reference: chr 11
allele count: 1
allele frequency: 8.689607229753214e-6
allele num: 115080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1804G>C
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-42C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-42C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-42C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-42C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-90C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-42C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-42C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1813C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-42C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-42C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-42C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-42C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-42C>G
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10329
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

11-65623756-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623756
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623756
    reference: chr 11
allele count: 1
allele frequency: 8.705493166187865e-6
allele num: 114870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-91C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1812C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1805G>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-43C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-43C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8450
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

11-65623759-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623759
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623759
    reference: chr 11
allele count: 5
allele frequency: 4.374453193350831e-5
allele num: 114300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-46G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-46G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-46G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-46G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-46G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-46G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-46G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-46G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-94G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1808C>T
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1809G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-46G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-46G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-46G>A
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9807
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD

11-65623763-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623763
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623763
    reference: chr 11
allele count: 1
allele frequency: 8.793991944703379e-6
allele num: 113714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-50G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1805G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-50G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-50G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-50G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-50G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-50G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1812C>T
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-50G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-50G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-98G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-50G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-50G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-50G>A
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9174
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-65623764-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623764
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623764
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 113578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-51G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-51G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1813C>A
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-51G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-51G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1804G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-51G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-51G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-99G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-51G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-51G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-51G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-51G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-51G>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-65623764-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623764
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623764
    reference: chr 11
allele count: 1
allele frequency: 8.804522002500484e-6
allele num: 113578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-51G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-51G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1804G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-51G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-51G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-51G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-99G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-51G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-51G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-51G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-51G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1813C>T
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-51G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-51G>A
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

11-65623765-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65623765
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65623765
    reference: chr 11
allele count: 1
allele frequency: 8.821142514378463e-6
allele num: 113364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-52G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+1803G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432226
  ensembl transcript: ENST00000524553
  gene symbol: CFL1
  hgvsc: ENST00000524553.1:c.-48-52G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436899
  ensembl transcript: ENST00000530413
  gene symbol: CFL1
  hgvsc: ENST00000530413.1:c.-100G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-48-52G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172803
  ensembl transcript: ENST00000530101
  gene symbol: SNX32
  hgvsc: ENST00000530101.1:n.1814C>T
  variant of: http://identifiers.org/hgnc/26423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.4-52G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-48-52G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432155
  ensembl transcript: ENST00000527344
  gene symbol: CFL1
  hgvsc: ENST00000527344.1:c.-48-52G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-52G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.99-52G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.4-52G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.4-52G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-52G>A
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8765
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum

11-65624865-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65624865
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65624865
    reference: chr 11
allele count: 3
allele frequency: 3.284431793299759e-4
allele num: 9134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+703C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-1152C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.-30G>A
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-49+238C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+703C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1152C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-350C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+703C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+703C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1152C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+703C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

11-65624869-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65624869
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65624869
    reference: chr 11
allele count: 1
allele frequency: 1.076889941847943e-4
allele num: 9286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1156C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+699C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.-26G>C
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+699C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+699C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-354C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-49+234C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+699C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-1156C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1156C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+699C>G
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.25e1
  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: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/11-65624885-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65624885
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65624885
    reference: chr 11
allele count: 1
allele frequency: 1.031778786628147e-4
allele num: 9692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-370G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-1172G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1172G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+683G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1172G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.-10C>A
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-49+218G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+683G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+683G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+683G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+683G>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  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: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3222
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

11-65624902-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65624902
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65624902
    reference: chr 11
allele count: 1
allele frequency: 1.011326860841424e-4
allele num: 9888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+666C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8G>A
  hgvsp: ENSP00000431979.1:p.Gly3Asp
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-387C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1189C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1189C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+666C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+666C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-1189C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+666C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+666C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-49+201C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly3Asp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-65624904-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65624904
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65624904
    reference: chr 11
allele count: 1
allele frequency: 1.010917913465427e-4
allele num: 9892
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1191A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-1191A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+664A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1191A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+2T>C
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-49+199A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-389A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+664A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+664A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+664A>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+664A>G
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  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: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
hgvs: c.8+2T>C
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

11-65624927-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65624927
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65624927
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 9886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-1214C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-49+176C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+641C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+641C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-412C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+641C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1214C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+25G>A
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+641C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+641C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1214C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  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 depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/11-65624934-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65624934
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65624934
    reference: chr 11
allele count: 6397
allele frequency: 6.301221434200157e-1
allele num: 10152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1221T>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+634T>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+634T>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1221T>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+32A>C
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+634T>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+634T>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-419T>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+634T>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-49+169T>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-1221T>G
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 2.5e0
  variant carriers: 344
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.25e1
  variant carriers: 573
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 2.25e1
  variant carriers: 927
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.25e1
  variant carriers: 431
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 390
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 266
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 2.75e1
  variant carriers: 814
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.75e1
  variant carriers: 773
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
  variant carriers: 130
num of homozygotes: 2026
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

11-65624937-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65624937
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65624937
    reference: chr 11
allele count: 4
allele frequency: 4.093327875562833e-4
allele num: 9772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-1224C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+631C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+631C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+35G>A
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-422C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+631C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1224C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+631C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+631C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-49+166C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1224C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

11-65624952-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65624952
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65624952
    reference: chr 11
allele count: 1
allele frequency: 1.069976460517869e-4
allele num: 9346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+50C>G
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+616G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+616G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433308
  ensembl transcript: ENST00000534784
  gene symbol: CFL1
  hgvsc: ENST00000534784.1:c.-437G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-48-1239G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+616G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433910
  ensembl transcript: ENST00000531407
  gene symbol: CFL1
  hgvsc: ENST00000531407.1:c.-49+151G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+616G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1239G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+616G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1239G>C
  variant of: http://identifiers.org/hgnc/1874
canonical: false
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ

11-65625520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625520
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625520
    reference: chr 11
allele count: 46
allele frequency: 3.574759092322039e-3
allele num: 12868
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1182G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+48G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+48G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+48G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1807G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1807G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+48G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+618C>T
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+48G>A
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4937
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

11-65625521-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625521
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625521
    reference: chr 11
allele count: 47
allele frequency: 3.634957463263728e-3
allele num: 12930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1181C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+619G>A
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+47C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1808C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+47C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+47C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+47C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1808C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+47C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4938
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2935
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1930
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 9.75e1
  variant carriers: 47
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/11-65625527-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625527
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625527
    reference: chr 11
allele count: 1
allele frequency: 7.819831091648421e-5
allele num: 12788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.98+41G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1175G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.3+41G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.61+41G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1814G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.3+41G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.3+41G>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+625C>A
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1814G>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4742
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3063
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1676
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

11-65625593-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625593
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625593
    reference: chr 11
allele count: 1
allele frequency: 6.688068485821294e-5
allele num: 14952
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.-23C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.36C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.-23C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.-23C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1880C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.73C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1880C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+691G>A
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1109C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3630
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

11-65625594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625594
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625594
    reference: chr 11
allele count: 1
allele frequency: 6.691648822269808e-5
allele num: 14944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.35C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1108C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.72C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.-24C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1881C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1881C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.-24C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+692G>A
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.-24C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1910
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

11-65625595-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625595
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625595
    reference: chr 11
allele count: 1
allele frequency: 6.68985817500669e-5
allele num: 14948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.34C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1882C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1107C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+693G>A
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.-25C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.71C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1882C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.-25C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.-25C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum

11-65625598-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625598
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625598
    reference: chr 11
allele count: 146
allele frequency: 9.704865727200213e-3
allele num: 15044
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1104G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+696C>G
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1885G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.31G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.-28G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.-28G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.-28G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1885G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.68G>C
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 7.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 9.75e1
  variant carriers: 129
genotype quality: GenotypeQuality
  all individuals: 3446
  bin: 7.5e0
  variant carriers: 2
num of homozygotes: 6
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

11-65625600-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625600
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625600
    reference: chr 11
allele count: 1
allele frequency: 6.64982045484772e-5
allele num: 15038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1887C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.-30C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.-30C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.66C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.-30C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.29C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+698G>A
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1102C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1887C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3441
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2293
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

11-65625600-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625600
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625600
    reference: chr 11
allele count: 1
allele frequency: 6.64982045484772e-5
allele num: 15038
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+698G>C
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1887C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.66C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.-30C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.-30C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.-30C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1887C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.29C>G
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1102C>G
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 939
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

11-65625602-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625602
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625602
    reference: chr 11
allele count: 1
allele frequency: 6.640106241699867e-5
allele num: 15060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1889C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.27C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.64C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1100C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.-32C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+700G>A
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.-32C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.-32C>T
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1889C>T
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3546
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2322
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

11-65625605-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625605
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625605
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 15010
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1892G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.-35G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1892G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.61G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.-35G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.24G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.-35G>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+703C>G
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1097G>C
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: 5' UTR
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3449
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

11-65625605-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625605
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625605
    reference: chr 11
allele count: 1
allele frequency: 6.662225183211193e-5
allele num: 15010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+703C>T
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1892G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.-35G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.-35G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.61G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.24G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1097G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1892G>A
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3449
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

11-65625606-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625606
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625606
    reference: chr 11
allele count: 1
allele frequency: 6.659563132658497e-5
allele num: 15016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.-36G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432153
  ensembl transcript: ENST00000526975
  gene symbol: CFL1
  hgvsc: ENST00000526975.1:c.-36G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172732
  ensembl protein: ENSP00000431979
  ensembl transcript: ENST00000529857
  gene symbol: MUS81
  hgvsc: ENST00000529857.1:c.8+704C>T
  variant of: http://identifiers.org/hgnc/29814
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1096G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000527752
  gene symbol: CFL1
  hgvsc: ENST00000527752.1:n.23G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172757
  ensembl transcript: ENST00000530945
  gene symbol: CFL1
  hgvsc: ENST00000530945.1:n.60G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000431696
  ensembl transcript: ENST00000534769
  gene symbol: CFL1
  hgvsc: ENST00000534769.1:c.118-1893G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1893G>A
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.-36G>A
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3432
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

11-65625609-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65625609
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65625609
    reference: chr 11
allele count: 1
allele frequency: 6.681812107443539e-5
allele num: 14966
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000309629
  ensembl transcript: ENST00000308162
  gene symbol: CFL1
  hgvsc: ENST00000308162.5:c.-39T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000432660
  ensembl transcript: ENST00000525451
  gene symbol: CFL1
  hgvsc: ENST00000525451.2:c.-39T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000436431
  ensembl transcript: ENST00000532134
  gene symbol: CFL1
  hgvsc: ENST00000532134.1:c.4-1896T>C
  variant of: http://identifiers.org/hgnc/1874
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172757
  ensembl protein: ENSP00000433131
  ensembl transcript: ENST00000531413
  gene symbol: CFL1
  hgvsc: ENST00000531413.1:c.-49+1093T>C
  variant of: http://identifiers.org/hgnc/1874
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 2940
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2423
bin: 6.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1825
bin: 6.75e1
variant carriers: 4

GenotypeDepth
all individuals: 10910
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 797
bin: 8.25e1
variant carriers: 15

GenotypeDepth
all individuals: 7833
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1653
bin: 9.75e1
variant carriers: 329

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

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5726
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3696
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1806
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4056
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3187
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24622
bin: 9.75e1
variant carriers: 386

East Asian
type: Population
allele count: 117
allele frequency: 1.351975964871736e-2
allele num: 8654
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 35
allele frequency: 5.244231345519928e-4
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.804920238324044e-4
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 202
allele frequency: 1.223352713178294e-2
allele num: 16512
num of homozygotes: 6

Latino
type: Population
allele count: 4
allele frequency: 3.454828122300915e-4
allele num: 11578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 28
allele frequency: 4.233444209253099e-3
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.414e0

FS
type: SiteQuality
SIO_000300: 5.19e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 2.672878e6

VQSLOD
type: SiteQuality
SIO_000300: 4.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.36e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.02e-1

QD
type: SiteQuality
SIO_000300: 1.329e1

GenotypeDepth
all individuals: 1328
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2955
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 782
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1829
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7876
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 526
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11316
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5775
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15301
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4089
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3714
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24347
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2441
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1813
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.17e-1

DP
type: SiteQuality
SIO_000300: 2.636211e6

FS
type: SiteQuality
SIO_000300: 2.81e0

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

GenotypeDepth
all individuals: 11316
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1437
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1332
bin: 9.75e1
variant carriers: 7

GenotypeDepth
all individuals: 7875
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3851
bin: 5.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 1029
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3714
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5776
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 24347
bin: 9.75e1
variant carriers: 9

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

GenotypeQuality
all individuals: 2441
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1813
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4088
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15301
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 7.68787238131847e-4
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.636616e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.919e0

QD
type: SiteQuality
SIO_000300: 1.397e1

FS
type: SiteQuality
SIO_000300: 1.113e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
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SIO_000300: 5.29e-1

ReadPosRankSum
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SIO_000300: 1.54e-1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

South Asian
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allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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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

DP
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QD
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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MQ
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FS
type: SiteQuality
SIO_000300: 5.27e-1

ClippingRankSum
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SIO_000300: -7.099999999999999e-2

ReadPosRankSum
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SIO_000300: 1.17e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
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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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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

DP
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SIO_000300: 2.635317e6

VQSLOD
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ReadPosRankSum
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SIO_000300: -3.16e-1

InbreedingCoeff
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MQRankSum
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SIO_000300: -9.419999999999999e-1

FS
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SIO_000300: 0.0e0

MQ
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SIO_000300: 5.976e1

ClippingRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

DP
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FS
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
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MQRankSum
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MQ
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SIO_000300: 5.867e1

ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 11

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

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

South Asian
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allele count: 12
allele frequency: 7.267441860465116e-4
allele num: 16512
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European (Non-Finnish)
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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

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele num: 66738
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African
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Latino
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East Asian
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MQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
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Latino
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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Other
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European (Non-Finnish)
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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DP
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QD
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BaseQRankSum
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MQRankSum
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FS
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GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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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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Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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African
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Other
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DP
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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QD
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VQSLOD
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FS
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

Other
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Latino
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allele frequency: 0.0e0
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South Asian
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African
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East Asian
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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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DP
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FS
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
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South Asian
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allele frequency: 0.0e0
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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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FS
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ReadPosRankSum
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MQ
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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MQRankSum
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 66734
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Other
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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Latino
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South Asian
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MQ
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QD
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MQRankSum
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VQSLOD
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FS
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DP
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

GenotypeDepth
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

DP
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SIO_000300: 2.632401e6

VQSLOD
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SIO_000300: 8.44e-1

ReadPosRankSum
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SIO_000300: 3.15e-1

FS
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QD
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ClippingRankSum
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SIO_000300: 1.22e-1

MQRankSum
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MQ
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SIO_000300: 5.943e1

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: -1.18e-1

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.497616263380409e-5
allele num: 66702
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.631473e6

MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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FS
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QD
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MQ
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SIO_000300: 5.979e1

VQSLOD
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SIO_000300: 1.12e0

ReadPosRankSum
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SIO_000300: 8.68e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.923446816695518e-4
allele num: 10398
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.303e1

BaseQRankSum
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SIO_000300: 2.26e0

FS
type: SiteQuality
SIO_000300: 2.467e0

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

MQRankSum
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SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 2.629113e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.75e-1

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

MQ
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SIO_000300: 5.904e1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.024e1

BaseQRankSum
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SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 6.028e0

VQSLOD
type: SiteQuality
SIO_000300: -6.937e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Latino
type: Population
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

African
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allele count: 1
allele frequency: 9.710623422023694e-5
allele num: 10298
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 count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 9.77e-1

MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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ClippingRankSum
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QD
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MQ
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SIO_000300: 5.97e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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DP
type: SiteQuality
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BaseQRankSum
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MQ
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QD
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MQRankSum
type: SiteQuality
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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SIO_000300: -1.42e-1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 33

GenotypeQuality
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variant carriers: 0

African
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allele count: 33
allele frequency: 3.230859604464461e-3
allele num: 10214
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66102
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European (Finnish)
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East Asian
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Latino
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South Asian
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QD
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FS
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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European (Finnish)
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DP
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VQSLOD
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FS
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3853
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3168
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10004
num of homozygotes: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 4.664800746368119e-4
allele num: 15006
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65476
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.08e-1

DP
type: SiteQuality
SIO_000300: 2.527645e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 6.850000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

QD
type: SiteQuality
SIO_000300: 1.548e1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-2

GenotypeDepth
all individuals: 3850
bin: 5.25e1
variant carriers: 2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 1789
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variant carriers: 0

GenotypeQuality
all individuals: 3168
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.138952164009112e-3
allele num: 878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.055954527396632e-5
allele num: 65446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14882
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.12e-1

FS
type: SiteQuality
SIO_000300: 2.732e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e0

QD
type: SiteQuality
SIO_000300: 1.39e1

DP
type: SiteQuality
SIO_000300: 2.527474e6

GenotypeDepth
all individuals: 496
bin: 8.75e1
variant carriers: 366

GenotypeDepth
all individuals: 2299
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variant carriers: 1479

GenotypeDepth
all individuals: 1386
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variant carriers: 1010

GenotypeDepth
all individuals: 1310
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variant carriers: 1072

GenotypeDepth
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variant carriers: 511

GenotypeQuality
all individuals: 99
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GenotypeQuality
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variant carriers: 15805

GenotypeQuality
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bin: 4.75e1
variant carriers: 29

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 24

GenotypeQuality
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variant carriers: 23

GenotypeQuality
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variant carriers: 31

GenotypeQuality
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variant carriers: 47

GenotypeQuality
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GenotypeQuality
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variant carriers: 23

GenotypeQuality
all individuals: 97
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variant carriers: 12

GenotypeQuality
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variant carriers: 37

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 8

GenotypeQuality
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variant carriers: 12

GenotypeQuality
all individuals: 3170
bin: 2.25e1
variant carriers: 17

GenotypeQuality
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bin: 4.25e1
variant carriers: 23

GenotypeQuality
all individuals: 2719
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variant carriers: 60

GenotypeQuality
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variant carriers: 26

GenotypeQuality
all individuals: 1587
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variant carriers: 39

GenotypeQuality
all individuals: 3558
bin: 7.75e1
variant carriers: 40

African
type: Population
allele count: 750
allele frequency: 7.527097551184263e-2
allele num: 9964
num of homozygotes: 29

European (Non-Finnish)
type: Population
allele count: 12478
allele frequency: 1.909703091521273e-1
allele num: 65340
num of homozygotes: 1229

East Asian
type: Population
allele count: 482
allele frequency: 5.590350266759453e-2
allele num: 8622
num of homozygotes: 12

South Asian
type: Population
allele count: 1348
allele frequency: 9.106877448993379e-2
allele num: 14802
num of homozygotes: 72

European (Finnish)
type: Population
allele count: 1013
allele frequency: 1.532062915910466e-1
allele num: 6612
num of homozygotes: 84

Latino
type: Population
allele count: 1460
allele frequency: 1.26648160999306e-1
allele num: 11528
num of homozygotes: 100

Other
type: Population
allele count: 146
allele frequency: 1.670480549199085e-1
allele num: 874
num of homozygotes: 14

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.513152e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.87e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.75e0

QD
type: SiteQuality
SIO_000300: 1.726e1

GenotypeDepth
all individuals: 4650
bin: 4.75e1
variant carriers: 7

GenotypeDepth
all individuals: 384
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variant carriers: 2

GenotypeDepth
all individuals: 534
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variant carriers: 4

GenotypeDepth
all individuals: 127
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variant carriers: 1

GenotypeDepth
all individuals: 1145
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variant carriers: 3

GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 5943
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variant carriers: 0

GenotypeQuality
all individuals: 996
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variant carriers: 0

GenotypeQuality
all individuals: 2141
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variant carriers: 0

GenotypeQuality
all individuals: 69
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variant carriers: 0

GenotypeQuality
all individuals: 3629
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variant carriers: 0

GenotypeQuality
all individuals: 916
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variant carriers: 0

GenotypeQuality
all individuals: 4823
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variant carriers: 0

GenotypeQuality
all individuals: 2794
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variant carriers: 0

GenotypeQuality
all individuals: 129
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variant carriers: 0

GenotypeQuality
all individuals: 123
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variant carriers: 0

GenotypeQuality
all individuals: 128
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variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 68
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 12938
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16395
bin: 9.75e1
variant carriers: 48

GenotypeQuality
all individuals: 4370
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 38
allele frequency: 5.844175817415644e-4
allele num: 65022
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.011122345803842e-4
allele num: 9890
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.847645429362881e-4
allele num: 14440
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.735809755250825e-4
allele num: 11522
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.132e0

VQSLOD
type: SiteQuality
SIO_000300: 5.11e0

DP
type: SiteQuality
SIO_000300: 2.166195e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.273e1

GenotypeDepth
all individuals: 1769
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2941
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 381
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variant carriers: 0

GenotypeDepth
all individuals: 531
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variant carriers: 1

GenotypeDepth
all individuals: 1938
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GenotypeQuality
all individuals: 5936
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variant carriers: 0

GenotypeQuality
all individuals: 2142
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variant carriers: 0

GenotypeQuality
all individuals: 554
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GenotypeQuality
all individuals: 90
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GenotypeQuality
all individuals: 4825
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variant carriers: 0

GenotypeQuality
all individuals: 144
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1042
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variant carriers: 0

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 940
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variant carriers: 0

GenotypeQuality
all individuals: 131
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 16360
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variant carriers: 6

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14404
num of homozygotes: 0

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

African
type: Population
allele count: 6
allele frequency: 6.075334143377885e-4
allele num: 9876
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64968
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

DP
type: SiteQuality
SIO_000300: 2.162176e6

MQRankSum
type: SiteQuality
SIO_000300: 3.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-1

FS
type: SiteQuality
SIO_000300: 1.495e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.01e-1

QD
type: SiteQuality
SIO_000300: 1.497e1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

GenotypeDepth
all individuals: 268
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 531
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variant carriers: 1

GenotypeDepth
all individuals: 9248
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variant carriers: 0

GenotypeDepth
all individuals: 365
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variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
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variant carriers: 0

GenotypeQuality
all individuals: 183
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GenotypeQuality
all individuals: 2786
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variant carriers: 0

GenotypeQuality
all individuals: 4224
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 2142
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 3631
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GenotypeQuality
all individuals: 5860
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GenotypeQuality
all individuals: 16356
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GenotypeQuality
all individuals: 180
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GenotypeQuality
all individuals: 140
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GenotypeQuality
all individuals: 4823
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GenotypeQuality
all individuals: 12389
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GenotypeQuality
all individuals: 451
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GenotypeQuality
all individuals: 645
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GenotypeQuality
all individuals: 90
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GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 4372
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64900
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14344
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 7.12e-1

FS
type: SiteQuality
SIO_000300: 5.831e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.26e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.649e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.31e0

MQRankSum
type: SiteQuality
SIO_000300: -2.422e0

VQSLOD
type: SiteQuality
SIO_000300: -2.047e0

DP
type: SiteQuality
SIO_000300: 2.155909e6

GenotypeDepth
all individuals: 365
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2936
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9153
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GenotypeDepth
all individuals: 126
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GenotypeDepth
all individuals: 268
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variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
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variant carriers: 0

GenotypeQuality
all individuals: 2762
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GenotypeQuality
all individuals: 2140
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GenotypeQuality
all individuals: 5662
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GenotypeQuality
all individuals: 261
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GenotypeQuality
all individuals: 290
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GenotypeQuality
all individuals: 16355
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GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 172
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GenotypeQuality
all individuals: 587
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GenotypeQuality
all individuals: 3627
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GenotypeQuality
all individuals: 11483
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GenotypeQuality
all individuals: 1053
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variant carriers: 0

GenotypeQuality
all individuals: 4060
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 886
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variant carriers: 0

GenotypeQuality
all individuals: 322
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GenotypeQuality
all individuals: 231
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GenotypeQuality
all individuals: 4362
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4800
bin: 7.75e1
variant carriers: 0

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

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

Latino
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South Asian
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East Asian
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African
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European (Non-Finnish)
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Other
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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Latino
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Other
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European (Non-Finnish)
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European (Finnish)
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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South Asian
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MQ
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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FS
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QD
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GenotypeDepth
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
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South Asian
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European (Finnish)
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Latino
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FS
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DP
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VQSLOD
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QD
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InbreedingCoeff
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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Latino
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East Asian
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South Asian
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BaseQRankSum
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FS
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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East Asian
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Latino
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VQSLOD
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ClippingRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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MQ
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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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African
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European (Non-Finnish)
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South Asian
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East Asian
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QD
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MQ
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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East Asian
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Other
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Latino
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European (Non-Finnish)
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DP
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VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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East Asian
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African
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Other
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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MQ
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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African
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Latino
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East Asian
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VQSLOD
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ClippingRankSum
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DP
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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East Asian
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Latino
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South Asian
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VQSLOD
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InbreedingCoeff
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DP
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FS
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ReadPosRankSum
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MQ
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GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 56
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.432664756446991e-4
allele num: 6980
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2402
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.843e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.48e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.058e0

FS
type: SiteQuality
SIO_000300: 1.685e0

DP
type: SiteQuality
SIO_000300: 1.25356e5

QD
type: SiteQuality
SIO_000300: 7.78e0

GenotypeQuality
all individuals: 52
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 197
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1939
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1964
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.75e1
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GenotypeQuality
all individuals: 121
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.22403e5

MQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.81e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.545e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.099e1

VQSLOD
type: SiteQuality
SIO_000300: 6.96e-1

GenotypeQuality
all individuals: 146
bin: 2.25e1
variant carriers: 70

GenotypeQuality
all individuals: 527
bin: 6.25e1
variant carriers: 200

GenotypeQuality
all individuals: 188
bin: 7.75e1
variant carriers: 153

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 125

GenotypeQuality
all individuals: 172
bin: 4.75e1
variant carriers: 155

GenotypeQuality
all individuals: 130
bin: 7.25e1
variant carriers: 108

GenotypeQuality
all individuals: 147
bin: 3.25e1
variant carriers: 97

GenotypeQuality
all individuals: 840
bin: 7.5e0
variant carriers: 227

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 110

GenotypeQuality
all individuals: 102
bin: 4.25e1
variant carriers: 86

GenotypeQuality
all individuals: 202
bin: 5.25e1
variant carriers: 193

GenotypeQuality
all individuals: 121
bin: 1.75e1
variant carriers: 115

GenotypeQuality
all individuals: 478
bin: 2.5e0
variant carriers: 6

GenotypeQuality
all individuals: 121
bin: 1.25e1
variant carriers: 107

GenotypeQuality
all individuals: 95
bin: 8.75e1
variant carriers: 91

GenotypeQuality
all individuals: 184
bin: 8.25e1
variant carriers: 161

GenotypeQuality
all individuals: 260
bin: 6.75e1
variant carriers: 203

GenotypeQuality
all individuals: 2638
bin: 9.75e1
variant carriers: 2618

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 45

Latino
type: Population
allele count: 55
allele frequency: 6.111111111111112e-1
allele num: 90
num of homozygotes: 15

South Asian
type: Population
allele count: 4538
allele frequency: 6.371805672563886e-1
allele num: 7122
num of homozygotes: 1457

African
type: Population
allele count: 64
allele frequency: 3.368421052631579e-1
allele num: 190
num of homozygotes: 13

East Asian
type: Population
allele count: 54
allele frequency: 4.090909090909091e-1
allele num: 132
num of homozygotes: 12

European (Non-Finnish)
type: Population
allele count: 1605
allele frequency: 6.42e-1
allele num: 2500
num of homozygotes: 502

Other
type: Population
allele count: 77
allele frequency: 6.875e-1
allele num: 112
num of homozygotes: 26

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.666666666666666e-1
allele num: 6
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.949e-1

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

DP
type: SiteQuality
SIO_000300: 1.41668e5

QD
type: SiteQuality
SIO_000300: 1.996e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
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variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 7.25e1
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GenotypeQuality
all individuals: 109
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 508
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 9.75e1
variant carriers: 4

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.807200929152149e-4
allele num: 6888
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2368
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.153e5

BaseQRankSum
type: SiteQuality
SIO_000300: -5.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.69e-1

FS
type: SiteQuality
SIO_000300: 4.304e0

QD
type: SiteQuality
SIO_000300: 1.476e1

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 201
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variant carriers: 0

GenotypeQuality
all individuals: 691
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variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2181
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 723
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variant carriers: 0

GenotypeQuality
all individuals: 500
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variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
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variant carriers: 1

GenotypeQuality
all individuals: 267
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.448398576512455e-4
allele num: 2248
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

VQSLOD
type: SiteQuality
SIO_000300: -2.839e0

DP
type: SiteQuality
SIO_000300: 1.09125e5

FS
type: SiteQuality
SIO_000300: 2.341e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.38e-2

QD
type: SiteQuality
SIO_000300: 2.933e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 382
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 213
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
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GenotypeQuality
all individuals: 464
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GenotypeQuality
all individuals: 2784
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variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1562
bin: 9.75e1
variant carriers: 44

GenotypeQuality
all individuals: 305
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

South Asian
type: Population
allele count: 46
allele frequency: 6.136606189967982e-3
allele num: 7496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4036
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.08e-1

FS
type: SiteQuality
SIO_000300: 9.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.47e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.317e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.085e0

DP
type: SiteQuality
SIO_000300: 2.18682e5

GenotypeQuality
all individuals: 133
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 977
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.75e1
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GenotypeQuality
all individuals: 333
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 187
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 695
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variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 9.25e1
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GenotypeQuality
all individuals: 1178
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

South Asian
type: Population
allele count: 47
allele frequency: 6.253326237360298e-3
allele num: 7516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4064
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.83e0

DP
type: SiteQuality
SIO_000300: 2.19533e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.38e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

QD
type: SiteQuality
SIO_000300: 1.26e1

GenotypeQuality
all individuals: 729
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 7.25e1
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GenotypeQuality
all individuals: 1538
bin: 9.75e1
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GenotypeQuality
all individuals: 68
bin: 5.25e1
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GenotypeQuality
all individuals: 415
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GenotypeQuality
all individuals: 193
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variant carriers: 1

GenotypeQuality
all individuals: 1360
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.525252525252525e-4
allele num: 3960
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7520
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.04e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.875e1

VQSLOD
type: SiteQuality
SIO_000300: -1.729e0

QD
type: SiteQuality
SIO_000300: 1.483e1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.36e-1

DP
type: SiteQuality
SIO_000300: 2.21714e5

GenotypeQuality
all individuals: 324
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2463
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5200
num of homozygotes: 0

African
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allele frequency: 8.403361344537816e-4
allele num: 1190
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7718
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 26
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 count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.624e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.53562e5

BaseQRankSum
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InbreedingCoeff
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SIO_000300: -3.76e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.205e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1186
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.926040061633282e-4
allele num: 5192
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7720
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.42e0

InbreedingCoeff
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SIO_000300: -3.86e-2

MQ
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SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.75e-1

FS
type: SiteQuality
SIO_000300: 4.177e0

DP
type: SiteQuality
SIO_000300: 2.53216e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele frequency: 0.0e0
allele num: 7718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.923076923076923e-4
allele num: 5200
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 428
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.015e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

QD
type: SiteQuality
SIO_000300: 1.075e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.21e-1

MQ
type: SiteQuality
SIO_000300: 5.644e1

DP
type: SiteQuality
SIO_000300: 2.53047e5

MQRankSum
type: SiteQuality
SIO_000300: 4.34e-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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variant carriers: 2

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.837298541826554e-4
allele num: 5212
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

African
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allele count: 141
allele frequency: 1.122611464968153e-1
allele num: 1256
num of homozygotes: 6

Latino
type: Population
allele count: 2
allele frequency: 8.130081300813009e-3
allele num: 246
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.295336787564767e-4
allele num: 7720
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.58e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

QD
type: SiteQuality
SIO_000300: 1.182e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.5488e5

VQSLOD
type: SiteQuality
SIO_000300: 5.71e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-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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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5222
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 6.578947368421052e-3
allele num: 152
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7722
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.034e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.77e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.39e-1

DP
type: SiteQuality
SIO_000300: 2.53905e5

BaseQRankSum
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.34e-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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European (Non-Finnish)
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allele count: 1
allele frequency: 1.914975105323631e-4
allele num: 5222
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
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Latino
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African
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num of homozygotes: 0

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

African
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South Asian
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allele frequency: 1.295001295001295e-4
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num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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South 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 num: 5200
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Latino
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DP
type: SiteQuality
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 205
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2182
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7726
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.920860545524395e-4
allele num: 5206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.53206e5

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

FS
type: SiteQuality
SIO_000300: 1.279e0

VQSLOD
type: SiteQuality
SIO_000300: -1.092e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.17e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.95e-1

MQ
type: SiteQuality
SIO_000300: 5.757e1

QD
type: SiteQuality
SIO_000300: 1.118e1