4-185687863-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687863
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687863
    reference: chr 4
allele count: 26835
allele frequency: 2.21173658616995e-1
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1074T>C
  hgvsp: ENST00000507295.1:c.1074T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1176T>C
  hgvsp: ENST00000504342.1:c.1176T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1176T>C
  hgvsp: ENST00000281455.2:c.1176T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*930T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.663T>C
  hgvsp: ENST00000437665.3:c.663T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1176T>C
  hgvsp: ENST00000515030.1:c.1176T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1176T>C
  hgvsp: ENST00000513317.1:c.1176T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.663T>C
  hgvsp: ENST00000454703.2:c.663T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9227
  bin: 3.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 2.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.25e1
  variant carriers: 579
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 5.75e1
  variant carriers: 481
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 7.25e1
  variant carriers: 833
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 4.75e1
  variant carriers: 296
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.25e1
  variant carriers: 232
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 3.75e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 5.25e1
  variant carriers: 376
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 9.25e1
  variant carriers: 1488
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 8.25e1
  variant carriers: 1081
genotype depth: GenotypeDepth
  all individuals: 17617
  bin: 2.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 15194
  bin: 9.75e1
  variant carriers: 15125
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 8.75e1
  variant carriers: 1339
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 6.75e1
  variant carriers: 652
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 7.75e1
  variant carriers: 941
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 8.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 6
hgvs: p.Phe392Phe
num of homozygotes: 3084
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-185687871-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687871
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687871
    reference: chr 4
allele count: 65
allele frequency: 5.359763840559395e-4
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1066T>C
  hgvsp: ENST00000507295.1:c.1066T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1168T>C
  hgvsp: ENST00000281455.2:c.1168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.655T>C
  hgvsp: ENST00000437665.3:c.655T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.655T>C
  hgvsp: ENST00000454703.2:c.655T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*922T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1168T>C
  hgvsp: ENST00000515030.1:c.1168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1168T>C
  hgvsp: ENST00000504342.1:c.1168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1168T>C
  hgvsp: ENST00000513317.1:c.1168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 15286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu390Leu
num of homozygotes: 1
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-185687879-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687879
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687879
    reference: chr 4
allele count: 2
allele frequency: 1.650028875505322e-5
allele num: 121210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*914G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1160G>T
  hgvsp: ENSP00000426150.1:p.Arg387Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.647G>T
  hgvsp: ENSP00000405687.3:p.Arg216Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1160G>T
  hgvsp: ENSP00000422607.1:p.Arg387Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1058G>T
  hgvsp: ENSP00000426244.1:p.Arg353Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1160G>T
  hgvsp: ENSP00000281455.2:p.Arg387Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1160G>T
  hgvsp: ENSP00000425006.1:p.Arg387Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.647G>T
  hgvsp: ENSP00000407165.2:p.Arg216Leu
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41837
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg387Leu
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: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

4-185687882-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687882
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687882
    reference: chr 4
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1157A>G
  hgvsp: ENSP00000281455.2:p.Lys386Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*911A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1055A>G
  hgvsp: ENSP00000426244.1:p.Lys352Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.644A>G
  hgvsp: ENSP00000405687.3:p.Lys215Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.644A>G
  hgvsp: ENSP00000407165.2:p.Lys215Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1157A>G
  hgvsp: ENSP00000425006.1:p.Lys386Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1157A>G
  hgvsp: ENSP00000426150.1:p.Lys386Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1157A>G
  hgvsp: ENSP00000422607.1:p.Lys386Arg
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8218
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1993
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1379
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys386Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

4-185687887-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687887
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687887
    reference: chr 4
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1050G>A
  hgvsp: ENST00000507295.1:c.1050G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1152G>A
  hgvsp: ENST00000281455.2:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1152G>A
  hgvsp: ENST00000513317.1:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*906G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.639G>A
  hgvsp: ENST00000454703.2:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1152G>A
  hgvsp: ENST00000504342.1:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1152G>A
  hgvsp: ENST00000515030.1:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.639G>A
  hgvsp: ENST00000437665.3:c.639G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15241
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr384Thr
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

4-185687888-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687888
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687888
    reference: chr 4
allele count: 4
allele frequency: 3.303218986902737e-5
allele num: 121094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.638C>T
  hgvsp: ENSP00000407165.2:p.Thr213Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1151C>T
  hgvsp: ENSP00000425006.1:p.Thr384Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.638C>T
  hgvsp: ENSP00000405687.3:p.Thr213Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1151C>T
  hgvsp: ENSP00000281455.2:p.Thr384Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*905C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1151C>T
  hgvsp: ENSP00000426150.1:p.Thr384Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1049C>T
  hgvsp: ENSP00000426244.1:p.Thr350Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1151C>T
  hgvsp: ENSP00000422607.1:p.Thr384Met
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2914
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41766
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr384Met
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

4-185687889-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687889
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687889
    reference: chr 4
allele count: 2
allele frequency: 1.651909607506277e-5
allele num: 121072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1048A>G
  hgvsp: ENSP00000426244.1:p.Thr350Ala
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1150A>G
  hgvsp: ENSP00000425006.1:p.Thr384Ala
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1150A>G
  hgvsp: ENSP00000426150.1:p.Thr384Ala
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.637A>G
  hgvsp: ENSP00000405687.3:p.Thr213Ala
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1150A>G
  hgvsp: ENSP00000281455.2:p.Thr384Ala
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1150A>G
  hgvsp: ENSP00000422607.1:p.Thr384Ala
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*904A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.637A>G
  hgvsp: ENSP00000407165.2:p.Thr213Ala
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2247
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41728
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr384Ala
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

4-185687900-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687900
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687900
    reference: chr 4
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1139A>G
  hgvsp: ENSP00000426150.1:p.Gln380Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.626A>G
  hgvsp: ENSP00000405687.3:p.Gln209Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*893A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1139A>G
  hgvsp: ENSP00000422607.1:p.Gln380Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.626A>G
  hgvsp: ENSP00000407165.2:p.Gln209Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1139A>G
  hgvsp: ENSP00000281455.2:p.Gln380Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1139A>G
  hgvsp: ENSP00000425006.1:p.Gln380Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1037A>G
  hgvsp: ENSP00000426244.1:p.Gln346Arg
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln380Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

4-185687901-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687901
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687901
    reference: chr 4
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1138C>G
  hgvsp: ENSP00000422607.1:p.Gln380Glu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.625C>G
  hgvsp: ENSP00000405687.3:p.Gln209Glu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1138C>G
  hgvsp: ENSP00000425006.1:p.Gln380Glu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1036C>G
  hgvsp: ENSP00000426244.1:p.Gln346Glu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1138C>G
  hgvsp: ENSP00000426150.1:p.Gln380Glu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.625C>G
  hgvsp: ENSP00000407165.2:p.Gln209Glu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1138C>G
  hgvsp: ENSP00000281455.2:p.Gln380Glu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*892C>G
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2904
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln380Glu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

4-185687904-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687904
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687904
    reference: chr 4
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1135G>A
  hgvsp: ENSP00000281455.2:p.Gly379Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1135G>A
  hgvsp: ENSP00000426150.1:p.Gly379Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1033G>A
  hgvsp: ENSP00000426244.1:p.Gly345Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1135G>A
  hgvsp: ENSP00000422607.1:p.Gly379Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.622G>A
  hgvsp: ENSP00000405687.3:p.Gly208Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1135G>A
  hgvsp: ENSP00000425006.1:p.Gly379Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.622G>A
  hgvsp: ENSP00000407165.2:p.Gly208Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*889G>A
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41149
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly379Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

4-185687905-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687905
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687905
    reference: chr 4
allele count: 3
allele frequency: 2.488593944421402e-5
allele num: 120550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1134C>T
  hgvsp: ENST00000504342.1:c.1134C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1134C>T
  hgvsp: ENST00000515030.1:c.1134C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1134C>T
  hgvsp: ENST00000513317.1:c.1134C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1134C>T
  hgvsp: ENST00000281455.2:c.1134C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1032C>T
  hgvsp: ENST00000507295.1:c.1032C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*888C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.621C>T
  hgvsp: ENST00000437665.3:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.621C>T
  hgvsp: ENST00000454703.2:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2198
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Phe378Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

4-185687918-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687918
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687918
    reference: chr 4
allele count: 1
allele frequency: 8.391514500537057e-6
allele num: 119168
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1129-8C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*883-8C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.616-8C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1129-8C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1129-8C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1129-8C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.616-8C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1027-8C>T
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2588
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1129-8C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP

4-185687919-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687919
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687919
    reference: chr 4
allele count: 2
allele frequency: 1.678500092317505e-5
allele num: 119154
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1129-9C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1129-9C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1027-9C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1129-9C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.616-9C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1129-9C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*883-9C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.616-9C>T
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14282
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

4-185687924-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687924
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687924
    reference: chr 4
allele count: 1
allele frequency: 8.43469019382918e-6
allele num: 118558
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*883-14T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.616-14T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1129-14T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1129-14T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1027-14T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1129-14T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.616-14T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1129-14T>C
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37742
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

4-185687942-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687942
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687942
    reference: chr 4
allele count: 6
allele frequency: 5.175447676223994e-5
allele num: 115932
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1129-32T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.616-32T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*883-32T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1027-32T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1129-32T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1129-32T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1129-32T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.616-32T>A
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18569
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8120
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7738
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-185687946-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687946
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687946
    reference: chr 4
allele count: 1
allele frequency: 8.671673112610347e-6
allele num: 115318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.616-36T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1129-36T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1129-36T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1027-36T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*883-36T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1129-36T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1129-36T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.616-36T>C
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5969
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4545
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5154
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3336
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5625
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

4-185687951-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687951
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687951
    reference: chr 4
allele count: 1
allele frequency: 8.770852702299717e-6
allele num: 114014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1027-41C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.616-41C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1129-41C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1129-41C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1129-41C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*883-41C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1129-41C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.616-41C>T
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15146
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2929
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7702
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6329
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2801
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

4-185687955-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687955
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687955
    reference: chr 4
allele count: 1
allele frequency: 8.866505887359909e-6
allele num: 112784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1129-45C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1027-45C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1129-45C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*883-45C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1129-45C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.616-45C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1129-45C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.616-45C>A
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15075
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6831
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2797
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3734
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7052
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

4-185687962-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185687962
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185687961
    reference: chr 4
allele count: 1
allele frequency: 9.070952994321584e-6
allele num: 110242
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1129-53delG
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.616-53delG
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1129-53delG
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.616-53delG
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1129-53delG
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1027-53delG
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*883-53delG
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1129-53delG
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14777
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10048
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13026
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7321
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5046
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1599
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6343
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6967
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: TC
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

4-185689387-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689387
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689387
    reference: chr 4
allele count: 2
allele frequency: 1.838269085828784e-5
allele num: 108798
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+83C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+83C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+83C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.*44C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+83C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+83C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+83C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+83C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+83C>T
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10135
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7012
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3387
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3692
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

4-185689391-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689391
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689392
    reference: chr 4
allele count: 10
allele frequency: 9.151810228063111e-5
allele num: 109268
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+78dupA
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+78dupA
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+78dupA
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+78dupA
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+78dupA
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+78dupA
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.*39dupA
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+78dupA
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+78dupA
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16371
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6671
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10527
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7732
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2885
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

4-185689393-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689393
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689393
    reference: chr 4
allele count: 1
allele frequency: 9.157173729900004e-6
allele num: 109204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+77C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+77C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+77C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+77C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+77C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+77C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+77C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+77C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16997
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15241
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2808
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-185689395-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689395
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689395
    reference: chr 4
allele count: 1
allele frequency: 9.148126463700234e-6
allele num: 109312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+75G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+75G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+75G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.*36G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+75G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+75G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+75G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+75G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+75G>T
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17579
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3176
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4630
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2545
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-185689400-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689400
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689400
    reference: chr 4
allele count: 1
allele frequency: 9.105312039043577e-6
allele num: 109826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+70G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+70G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+70G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.*31G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+70G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+70G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+70G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+70G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+70G>T
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7794
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18026
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4679
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3386
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

4-185689420-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689420
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689420
    reference: chr 4
allele count: 3
allele frequency: 2.631163500499921e-5
allele num: 114018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+50G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+50G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+50G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+50G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+50G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.*11G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+50G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+50G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+50G>A
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8797
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23048
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

4-185689424-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689424
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689424
    reference: chr 4
allele count: 42
allele frequency: 3.646909678203637e-4
allele num: 115166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.*7C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+46C>T
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 23524
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13561
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9012
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3105
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1897
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-185689435-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689435
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689435
    reference: chr 4
allele count: 1
allele frequency: 8.530530769624486e-6
allele num: 117226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+35A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+35A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+35A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1163A>G
  hgvsp: ENSP00000424935.1:p.His388Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+35A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+35A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+35A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+35A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+35A>G
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5153
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His388Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

4-185689436-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689436
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689436
    reference: chr 4
allele count: 1
allele frequency: 8.521516829995738e-6
allele num: 117350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+34C>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+34C>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1162C>G
  hgvsp: ENSP00000424935.1:p.His388Asp
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+34C>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+34C>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+34C>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+34C>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+34C>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+34C>G
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5156
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His388Asp
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

4-185689439-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689439
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689439
    reference: chr 4
allele count: 2
allele frequency: 1.695403760405541e-5
allele num: 117966
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+31G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+31G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+31G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1159G>A
  hgvsp: ENSP00000424935.1:p.Glu387Lys
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+31G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+31G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+31G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+31G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+31G>A
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4147
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu387Lys
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

4-185689444-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689444
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689444
    reference: chr 4
allele count: 2
allele frequency: 1.682680172979522e-5
allele num: 118858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+26G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+26G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+26G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+26G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+26G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1154G>A
  hgvsp: ENSP00000424935.1:p.Arg385Lys
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+26G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+26G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+26G>A
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9236
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg385Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

4-185689446-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689446
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689446
    reference: chr 4
allele count: 3
allele frequency: 2.516567402063585e-5
allele num: 119210
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+24C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+24C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+24C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+24C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+24C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1152C>A
  hgvsp: ENST00000504900.1:c.1152C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+24C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+24C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+24C>A
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9283
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1942
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8184
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro384Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

4-185689453-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689453
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689453
    reference: chr 4
allele count: 11
allele frequency: 9.164528276735428e-5
allele num: 120028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+17G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+17G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+17G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+17G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1145G>A
  hgvsp: ENSP00000424935.1:p.Arg382Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+17G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+17G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+17G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+17G>A
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8271
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg382Gln
num of homozygotes: 1
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-185689454-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689454
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689454
    reference: chr 4
allele count: 29
allele frequency: 2.410760303922058e-4
allele num: 120294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+16C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+16C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+16C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+16C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1144C>T
  hgvsp: ENSP00000424935.1:p.Arg382Ter
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+16C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+16C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+16C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+16C>T
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14382
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26166
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9421
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg382Ter
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-185689459-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689459
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689459
    reference: chr 4
allele count: 1
allele frequency: 8.272530236098013e-6
allele num: 120882
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+11A>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+11A>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+11A>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+11A>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1139A>C
  hgvsp: ENSP00000424935.1:p.Lys380Thr
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+11A>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+11A>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+11A>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+11A>C
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8247
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Lys380Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

4-185689466-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689466
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689466
    reference: chr 4
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1128+4A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1128+4A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.615+4A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*882+4A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1132A>G
  hgvsp: ENSP00000424935.1:p.Ser378Gly
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1128+4A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.615+4A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1128+4A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1026+4A>G
  variant of: http://identifiers.org/hgnc/3569
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser378Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

4-185689471-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689471
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689471
    reference: chr 4
allele count: 12
allele frequency: 9.898703269871646e-5
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1127G>A
  hgvsp: ENSP00000424935.1:p.Arg376Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*881G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1127G>A
  hgvsp: ENSP00000425006.1:p.Arg376Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1127G>A
  hgvsp: ENSP00000422607.1:p.Arg376Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1127G>A
  hgvsp: ENSP00000281455.2:p.Arg376Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.614G>A
  hgvsp: ENSP00000407165.2:p.Arg205Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.614G>A
  hgvsp: ENSP00000405687.3:p.Arg205Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1025G>A
  hgvsp: ENSP00000426244.1:p.Arg342Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1127G>A
  hgvsp: ENSP00000426150.1:p.Arg376Gln
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9607
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26418
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4356
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg376Gln
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

4-185689472-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689472
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689472
    reference: chr 4
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1126C>T
  hgvsp: ENSP00000424935.1:p.Arg376Ter
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1126C>T
  hgvsp: ENSP00000281455.2:p.Arg376Ter
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1126C>T
  hgvsp: ENSP00000426150.1:p.Arg376Ter
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.613C>T
  hgvsp: ENSP00000407165.2:p.Arg205Ter
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1024C>T
  hgvsp: ENSP00000426244.1:p.Arg342Ter
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1126C>T
  hgvsp: ENSP00000422607.1:p.Arg376Ter
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1126C>T
  hgvsp: ENSP00000425006.1:p.Arg376Ter
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*880C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.613C>T
  hgvsp: ENSP00000405687.3:p.Arg205Ter
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8276
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg376Ter
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-185689473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689473
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689473
    reference: chr 4
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1125C>T
  hgvsp: ENST00000281455.2:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1023C>T
  hgvsp: ENST00000507295.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.612C>T
  hgvsp: ENST00000437665.3:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1125C>T
  hgvsp: ENST00000504342.1:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*879C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1125C>T
  hgvsp: ENST00000515030.1:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1125C>T
  hgvsp: ENST00000513317.1:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1125C>T
  hgvsp: ENST00000504900.1:c.1125C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.612C>T
  hgvsp: ENST00000454703.2:c.612C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp375Asp
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/4-185689478-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689478
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689478
    reference: chr 4
allele count: 2
allele frequency: 1.648614339647526e-5
allele num: 121314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.607T>G
  hgvsp: ENSP00000407165.2:p.Phe203Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1120T>G
  hgvsp: ENSP00000425006.1:p.Phe374Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1120T>G
  hgvsp: ENSP00000281455.2:p.Phe374Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.607T>G
  hgvsp: ENSP00000405687.3:p.Phe203Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*874T>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1120T>G
  hgvsp: ENSP00000422607.1:p.Phe374Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1120T>G
  hgvsp: ENSP00000426150.1:p.Phe374Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1120T>G
  hgvsp: ENSP00000424935.1:p.Phe374Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1018T>G
  hgvsp: ENSP00000426244.1:p.Phe340Val
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe374Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ

4-185689480-A-AGT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689480
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689482
    reference: chr 4
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: AGT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.604_605insAC
  hgvsp: ENSP00000405687.3:p.Met202AsnfsTer14
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1117_1118insAC
  hgvsp: ENSP00000422607.1:p.Met373AsnfsTer14
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.604_605insAC
  hgvsp: ENSP00000407165.2:p.Met202AsnfsTer14
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1015_1016insAC
  hgvsp: ENSP00000426244.1:p.Met339AsnfsTer14
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1117_1118insAC
  hgvsp: ENSP00000281455.2:p.Met373AsnfsTer14
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1117_1118insAC
  hgvsp: ENSP00000426150.1:p.Met373AsnfsTer14
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*871_*872insAC
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1117_1118insAC
  hgvsp: ENSP00000425006.1:p.Met373AsnfsTer14
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1117_1118insAC
  hgvsp: ENSP00000424935.1:p.Met373AsnfsTer6
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8467
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Met373AsnfsTer14
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-185689482-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689482
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689482
    reference: chr 4
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1116G>A
  hgvsp: ENST00000513317.1:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1116G>A
  hgvsp: ENST00000504900.1:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.603G>A
  hgvsp: ENST00000454703.2:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1116G>A
  hgvsp: ENST00000515030.1:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1116G>A
  hgvsp: ENST00000504342.1:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.603G>A
  hgvsp: ENST00000437665.3:c.603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*870G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.280G>A
  hgvsp: ENST00000505492.1:c.280G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1116G>A
  hgvsp: ENST00000281455.2:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1014G>A
  hgvsp: ENST00000507295.1:c.1014G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25553
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg372Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/4-185689483-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689483
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689483
    reference: chr 4
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1115G>T
  hgvsp: ENSP00000424935.1:p.Arg372Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1115G>T
  hgvsp: ENSP00000422607.1:p.Arg372Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*869G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.602G>T
  hgvsp: ENSP00000405687.3:p.Arg201Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1115G>T
  hgvsp: ENSP00000281455.2:p.Arg372Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1013G>T
  hgvsp: ENSP00000426244.1:p.Arg338Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1115G>T
  hgvsp: ENSP00000425006.1:p.Arg372Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.602G>T
  hgvsp: ENSP00000407165.2:p.Arg201Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.279G>T
  hgvsp: ENSP00000425640.1:p.Arg94Leu
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1115G>T
  hgvsp: ENSP00000426150.1:p.Arg372Leu
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9670
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg372Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

4-185689483-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689483
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689483
    reference: chr 4
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1115G>A
  hgvsp: ENSP00000424935.1:p.Arg372Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1013G>A
  hgvsp: ENSP00000426244.1:p.Arg338Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1115G>A
  hgvsp: ENSP00000426150.1:p.Arg372Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1115G>A
  hgvsp: ENSP00000425006.1:p.Arg372Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1115G>A
  hgvsp: ENSP00000281455.2:p.Arg372Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.279G>A
  hgvsp: ENSP00000425640.1:p.Arg94Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.602G>A
  hgvsp: ENSP00000407165.2:p.Arg201Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.602G>A
  hgvsp: ENSP00000405687.3:p.Arg201Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1115G>A
  hgvsp: ENSP00000422607.1:p.Arg372Gln
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*869G>A
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9670
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25549
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg372Gln
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

4-185689493-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689493
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689493
    reference: chr 4
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*859C>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.592C>G
  hgvsp: ENSP00000407165.2:p.Leu198Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1105C>G
  hgvsp: ENSP00000281455.2:p.Leu369Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1105C>G
  hgvsp: ENSP00000425006.1:p.Leu369Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.592C>G
  hgvsp: ENSP00000405687.3:p.Leu198Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1105C>G
  hgvsp: ENSP00000426150.1:p.Leu369Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1105C>G
  hgvsp: ENSP00000424935.1:p.Leu369Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.269C>G
  hgvsp: ENSP00000425640.1:p.Leu91Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.1003C>G
  hgvsp: ENSP00000426244.1:p.Leu335Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1105C>G
  hgvsp: ENSP00000422607.1:p.Leu369Val
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu369Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

4-185689505-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689505
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689505
    reference: chr 4
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*847G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.580G>A
  hgvsp: ENSP00000405687.3:p.Val194Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1093G>A
  hgvsp: ENSP00000425006.1:p.Val365Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.580G>A
  hgvsp: ENSP00000407165.2:p.Val194Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1093G>A
  hgvsp: ENSP00000281455.2:p.Val365Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.991G>A
  hgvsp: ENSP00000426244.1:p.Val331Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1093G>A
  hgvsp: ENSP00000422607.1:p.Val365Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1093G>A
  hgvsp: ENSP00000424935.1:p.Val365Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1093G>A
  hgvsp: ENSP00000426150.1:p.Val365Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.257G>A
  hgvsp: ENSP00000425640.1:p.Val87Met
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val365Met
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

4-185689506-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689506
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689506
    reference: chr 4
allele count: 26
allele frequency: 2.141609831636519e-4
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.990C>T
  hgvsp: ENST00000507295.1:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1092C>T
  hgvsp: ENST00000515030.1:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1092C>T
  hgvsp: ENST00000504342.1:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.579C>T
  hgvsp: ENST00000437665.3:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.579C>T
  hgvsp: ENST00000454703.2:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1092C>T
  hgvsp: ENST00000281455.2:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.256C>T
  hgvsp: ENST00000505492.1:c.256C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*846C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1092C>T
  hgvsp: ENST00000504900.1:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1092C>T
  hgvsp: ENST00000513317.1:c.1092C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro364Pro
num of homozygotes: 1
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-185689527-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689527
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689527
    reference: chr 4
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1071G>A
  hgvsp: ENST00000515030.1:c.1071G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1071G>A
  hgvsp: ENST00000504342.1:c.1071G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1071G>A
  hgvsp: ENST00000281455.2:c.1071G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.969G>A
  hgvsp: ENST00000507295.1:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.558G>A
  hgvsp: ENST00000437665.3:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.558G>A
  hgvsp: ENST00000454703.2:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1071G>A
  hgvsp: ENST00000504900.1:c.1071G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.235G>A
  hgvsp: ENST00000505492.1:c.235G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1071G>A
  hgvsp: ENST00000513317.1:c.1071G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*825G>A
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4390
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val357Val
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS

4-185689529-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689529
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689529
    reference: chr 4
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.556G>A
  hgvsp: ENSP00000407165.2:p.Val186Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.233G>A
  hgvsp: ENSP00000425640.1:p.Val79Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.556G>A
  hgvsp: ENSP00000405687.3:p.Val186Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1069G>A
  hgvsp: ENSP00000425006.1:p.Val357Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1069G>A
  hgvsp: ENSP00000426150.1:p.Val357Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*823G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1069G>A
  hgvsp: ENSP00000281455.2:p.Val357Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1069G>A
  hgvsp: ENSP00000422607.1:p.Val357Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.967G>A
  hgvsp: ENSP00000426244.1:p.Val323Met
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1069G>A
  hgvsp: ENSP00000424935.1:p.Val357Met
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val357Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

4-185689531-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689531
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689531
    reference: chr 4
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1067A>G
  hgvsp: ENSP00000424935.1:p.Lys356Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1067A>G
  hgvsp: ENSP00000426150.1:p.Lys356Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.554A>G
  hgvsp: ENSP00000405687.3:p.Lys185Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1067A>G
  hgvsp: ENSP00000422607.1:p.Lys356Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1067A>G
  hgvsp: ENSP00000281455.2:p.Lys356Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.965A>G
  hgvsp: ENSP00000426244.1:p.Lys322Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.554A>G
  hgvsp: ENSP00000407165.2:p.Lys185Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1067A>G
  hgvsp: ENSP00000425006.1:p.Lys356Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*821A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.231A>G
  hgvsp: ENSP00000425640.1:p.Lys78Arg
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys356Arg
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: T
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

4-185689533-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689533
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689533
    reference: chr 4
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*819C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.229C>T
  hgvsp: ENST00000505492.1:c.229C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.552C>T
  hgvsp: ENST00000437665.3:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1065C>T
  hgvsp: ENST00000504342.1:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.552C>T
  hgvsp: ENST00000454703.2:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1065C>T
  hgvsp: ENST00000281455.2:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.963C>T
  hgvsp: ENST00000507295.1:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1065C>T
  hgvsp: ENST00000515030.1:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1065C>T
  hgvsp: ENST00000513317.1:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1065C>T
  hgvsp: ENST00000504900.1:c.1065C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu355Leu
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-185689533-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689533
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689533
    reference: chr 4
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.963C>G
  hgvsp: ENST00000507295.1:c.963C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.229C>G
  hgvsp: ENST00000505492.1:c.229C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1065C>G
  hgvsp: ENST00000281455.2:c.1065C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1065C>G
  hgvsp: ENST00000504900.1:c.1065C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*819C>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1065C>G
  hgvsp: ENST00000515030.1:c.1065C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1065C>G
  hgvsp: ENST00000504342.1:c.1065C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1065C>G
  hgvsp: ENST00000513317.1:c.1065C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.552C>G
  hgvsp: ENST00000454703.2:c.552C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.552C>G
  hgvsp: ENST00000437665.3:c.552C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu355Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

4-185689540-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689540
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689540
    reference: chr 4
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1058A>G
  hgvsp: ENSP00000426150.1:p.Asp353Gly
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1058A>G
  hgvsp: ENSP00000281455.2:p.Asp353Gly
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.956A>G
  hgvsp: ENSP00000426244.1:p.Asp319Gly
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1058A>G
  hgvsp: ENSP00000424935.1:p.Asp353Gly
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1058A>G
  hgvsp: ENSP00000425006.1:p.Asp353Gly
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.545A>G
  hgvsp: ENSP00000405687.3:p.Asp182Gly
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1058A>G
  hgvsp: ENSP00000422607.1:p.Asp353Gly
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*812A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.222A>G
  hgvsp: ENSP00000425640.1:p.Asp75Gly
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.545A>G
  hgvsp: ENSP00000407165.2:p.Asp182Gly
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp353Gly
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD

4-185689551-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689551
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689551
    reference: chr 4
allele count: 6
allele frequency: 4.941932295527551e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.945G>A
  hgvsp: ENST00000507295.1:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.211G>A
  hgvsp: ENST00000505492.1:c.211G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1047G>A
  hgvsp: ENST00000504342.1:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1047G>A
  hgvsp: ENST00000515030.1:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.534G>A
  hgvsp: ENST00000454703.2:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.534G>A
  hgvsp: ENST00000437665.3:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1047G>A
  hgvsp: ENST00000513317.1:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1047G>A
  hgvsp: ENST00000504900.1:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1047G>A
  hgvsp: ENST00000281455.2:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*801G>A
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 26322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg349Arg
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: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP

4-185689575-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689575
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689575
    reference: chr 4
allele count: 5
allele frequency: 4.11820907323823e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1023C>T
  hgvsp: ENST00000504900.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.921C>T
  hgvsp: ENST00000507295.1:c.921C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1023C>T
  hgvsp: ENST00000515030.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1023C>T
  hgvsp: ENST00000504342.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1023C>T
  hgvsp: ENST00000513317.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.510C>T
  hgvsp: ENST00000437665.3:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.187C>T
  hgvsp: ENST00000505492.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1023C>T
  hgvsp: ENST00000281455.2:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*777C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.510C>T
  hgvsp: ENST00000454703.2:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9705
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25526
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile341Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

4-185689581-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689581
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689581
    reference: chr 4
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.181T>C
  hgvsp: ENST00000505492.1:c.181T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.504T>C
  hgvsp: ENST00000437665.3:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1017T>C
  hgvsp: ENST00000515030.1:c.1017T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*771T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.915T>C
  hgvsp: ENST00000507295.1:c.915T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1017T>C
  hgvsp: ENST00000281455.2:c.1017T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1017T>C
  hgvsp: ENST00000513317.1:c.1017T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1017T>C
  hgvsp: ENST00000504900.1:c.1017T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.504T>C
  hgvsp: ENST00000454703.2:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1017T>C
  hgvsp: ENST00000504342.1:c.1017T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4389
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala339Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

4-185689582-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689582
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689582
    reference: chr 4
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1016C>T
  hgvsp: ENSP00000425006.1:p.Ala339Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1016C>T
  hgvsp: ENSP00000424935.1:p.Ala339Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*770C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1016C>T
  hgvsp: ENSP00000422607.1:p.Ala339Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.180C>T
  hgvsp: ENSP00000425640.1:p.Ala61Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.503C>T
  hgvsp: ENSP00000407165.2:p.Ala168Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.503C>T
  hgvsp: ENSP00000405687.3:p.Ala168Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.914C>T
  hgvsp: ENSP00000426244.1:p.Ala305Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1016C>T
  hgvsp: ENSP00000426150.1:p.Ala339Val
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1016C>T
  hgvsp: ENSP00000281455.2:p.Ala339Val
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9705
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2580
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala339Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

4-185689583-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689583
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689583
    reference: chr 4
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1015G>C
  hgvsp: ENSP00000426150.1:p.Ala339Pro
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.502G>C
  hgvsp: ENSP00000405687.3:p.Ala168Pro
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.913G>C
  hgvsp: ENSP00000426244.1:p.Ala305Pro
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.179G>C
  hgvsp: ENSP00000425640.1:p.Ala61Pro
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*769G>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1015G>C
  hgvsp: ENSP00000281455.2:p.Ala339Pro
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1015G>C
  hgvsp: ENSP00000422607.1:p.Ala339Pro
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1015G>C
  hgvsp: ENSP00000425006.1:p.Ala339Pro
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.502G>C
  hgvsp: ENSP00000407165.2:p.Ala168Pro
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1015G>C
  hgvsp: ENSP00000424935.1:p.Ala339Pro
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala339Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

4-185689588-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689588
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689588
    reference: chr 4
allele count: 5
allele frequency: 4.11820907323823e-5
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.497A>G
  hgvsp: ENSP00000407165.2:p.His166Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1010A>G
  hgvsp: ENSP00000426150.1:p.His337Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1010A>G
  hgvsp: ENSP00000281455.2:p.His337Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1010A>G
  hgvsp: ENSP00000422607.1:p.His337Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.174A>G
  hgvsp: ENSP00000425640.1:p.His59Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*764A>G
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1010A>G
  hgvsp: ENSP00000425006.1:p.His337Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1010A>G
  hgvsp: ENSP00000424935.1:p.His337Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.497A>G
  hgvsp: ENSP00000405687.3:p.His166Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.908A>G
  hgvsp: ENSP00000426244.1:p.His303Arg
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14705
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His337Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

4-185689595-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689595
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689595
    reference: chr 4
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.167C>T
  hgvsp: ENST00000505492.1:c.167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.490C>T
  hgvsp: ENST00000437665.3:c.490C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.1003C>T
  hgvsp: ENST00000513317.1:c.1003C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.1003C>T
  hgvsp: ENST00000515030.1:c.1003C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.901C>T
  hgvsp: ENST00000507295.1:c.901C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.1003C>T
  hgvsp: ENST00000504342.1:c.1003C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.1003C>T
  hgvsp: ENST00000281455.2:c.1003C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.490C>T
  hgvsp: ENST00000454703.2:c.490C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.1003C>T
  hgvsp: ENST00000504900.1:c.1003C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*757C>T
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu335Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

4-185689604-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689604
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689604
    reference: chr 4
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.994T>C
  hgvsp: ENSP00000281455.2:p.Cys332Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.994T>C
  hgvsp: ENSP00000426150.1:p.Cys332Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.994T>C
  hgvsp: ENSP00000422607.1:p.Cys332Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*748T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.994T>C
  hgvsp: ENSP00000424935.1:p.Cys332Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.481T>C
  hgvsp: ENSP00000407165.2:p.Cys161Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.481T>C
  hgvsp: ENSP00000405687.3:p.Cys161Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.994T>C
  hgvsp: ENSP00000425006.1:p.Cys332Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.892T>C
  hgvsp: ENSP00000426244.1:p.Cys298Arg
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.158T>C
  hgvsp: ENSP00000425640.1:p.Cys54Arg
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys332Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

4-185689617-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689617
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689616
    reference: chr 4
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*748-14delC
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.994-14delC
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.158-14delC
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.994-14delC
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.481-14delC
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.892-14delC
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.994-14delC
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.994-14delC
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.994-14delC
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.481-14delC
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14705
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9700
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: TG
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

4-185689620-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689620
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689620
    reference: chr 4
allele count: 6
allele frequency: 4.942420797706717e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.994-16T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.994-16T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.994-16T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.481-16T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.994-16T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.994-16T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.892-16T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.158-16T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.481-16T>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*748-16T>A
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8363
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 8493
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

4-185689631-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689631
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689631
    reference: chr 4
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.994-27T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.994-27T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.994-27T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*748-27T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.158-27T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.481-27T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.994-27T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.994-27T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.481-27T>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.892-27T>C
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3871
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

4-185689640-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689640
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689640
    reference: chr 4
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.994-36G>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*748-36G>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.994-36G>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.892-36G>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.158-36G>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.994-36G>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.994-36G>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.481-36G>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.481-36G>C
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.994-36G>C
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4388
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8366
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum

4-185689640-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689640
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689640
    reference: chr 4
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.994-36G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.994-36G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.481-36G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.481-36G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.994-36G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*748-36G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.158-36G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.994-36G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.892-36G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.994-36G>A
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-185689643-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689643
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689643
    reference: chr 4
allele count: 13
allele frequency: 1.071104885886133e-4
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.481-39G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.994-39G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.994-39G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.994-39G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.892-39G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.481-39G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*748-39G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.994-39G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.158-39G>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.994-39G>T
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2576
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

4-185689646-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689646
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689646
    reference: chr 4
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*748-42G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.994-42G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.994-42G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.481-42G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.481-42G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.994-42G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.892-42G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.994-42G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.158-42G>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.994-42G>A
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8378
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8443
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

4-185689650-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689650
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689650
    reference: chr 4
allele count: 3
allele frequency: 2.472187886279357e-5
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.994-46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.481-46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.994-46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.994-46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.994-46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.994-46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.892-46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.481-46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.158-46C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*748-46C>T
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

4-185689651-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689651
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689651
    reference: chr 4
allele count: 3
allele frequency: 2.47222863170386e-5
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.994-47C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.892-47C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.994-47C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.158-47C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.481-47C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.994-47C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*748-47C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.481-47C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.994-47C>T
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.994-47C>T
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4385
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

4-185689651-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 185689651
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 185689651
    reference: chr 4
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425006
  ensembl transcript: ENST00000504342
  gene symbol: ACSL1
  hgvsc: ENST00000504342.1:c.994-47C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000407165
  ensembl transcript: ENST00000454703
  gene symbol: ACSL1
  hgvsc: ENST00000454703.2:c.481-47C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000424935
  ensembl transcript: ENST00000504900
  gene symbol: ACSL1
  hgvsc: ENST00000504900.1:c.994-47C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000422607
  ensembl transcript: ENST00000515030
  gene symbol: ACSL1
  hgvsc: ENST00000515030.1:c.994-47C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000405687
  ensembl transcript: ENST00000437665
  gene symbol: ACSL1
  hgvsc: ENST00000437665.3:c.481-47C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426244
  ensembl transcript: ENST00000507295
  gene symbol: ACSL1
  hgvsc: ENST00000507295.1:c.892-47C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000281455
  ensembl transcript: ENST00000281455
  gene symbol: ACSL1
  hgvsc: ENST00000281455.2:c.994-47C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426491
  ensembl transcript: ENST00000506733
  gene symbol: ACSL1
  hgvsc: ENST00000506733.1:c.*748-47C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000425640
  ensembl transcript: ENST00000505492
  gene symbol: ACSL1
  hgvsc: ENST00000505492.1:c.158-47C>A
  variant of: http://identifiers.org/hgnc/3569
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151726
  ensembl protein: ENSP00000426150
  ensembl transcript: ENST00000513317
  gene symbol: ACSL1
  hgvsc: ENST00000513317.1:c.994-47C>A
  variant of: http://identifiers.org/hgnc/3569
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 5223
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 511
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1222
bin: 7.25e1
variant carriers: 7

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1339
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 25556
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 369
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 25525
bin: 9.75e1
variant carriers: 23707

European (Non-Finnish)
type: Population
allele count: 15545
allele frequency: 2.329746418080451e-1
allele num: 66724
num of homozygotes: 1846

African
type: Population
allele count: 2298
allele frequency: 2.208341341533731e-1
allele num: 10406
num of homozygotes: 274

European (Finnish)
type: Population
allele count: 1162
allele frequency: 1.756879346840036e-1
allele num: 6614
num of homozygotes: 113

South Asian
type: Population
allele count: 3449
allele frequency: 2.094364828758805e-1
allele num: 16468
num of homozygotes: 375

Latino
type: Population
allele count: 2137
allele frequency: 1.846060815480304e-1
allele num: 11576
num of homozygotes: 214

East Asian
type: Population
allele count: 2035
allele frequency: 2.356960852443827e-1
allele num: 8634
num of homozygotes: 237

Other
type: Population
allele count: 209
allele frequency: 2.301762114537445e-1
allele num: 908
num of homozygotes: 25

FS
type: SiteQuality
SIO_000300: 6.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.26e0

DP
type: SiteQuality
SIO_000300: 3.658289e6

QD
type: SiteQuality
SIO_000300: 1.711e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.38e-1

GenotypeQuality
all individuals: 2989
bin: 9.75e1
variant carriers: 64

GenotypeQuality
all individuals: 41858
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8652
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2256
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
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: 908
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
type: Population
allele count: 65
allele frequency: 3.956177723676202e-3
allele num: 16430
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.801643e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.21e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.89e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.0e-3

GenotypeQuality
all individuals: 2257
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 817
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8659
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 5.96e-1

FS
type: SiteQuality
SIO_000300: 1.098e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.135e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.602e1

DP
type: SiteQuality
SIO_000300: 1.796704e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.49e0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41807
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2919
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 8651
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 5.945e1

VQSLOD
type: SiteQuality
SIO_000300: -1.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.766e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

FS
type: SiteQuality
SIO_000300: 4.955e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.795812e6

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

GenotypeQuality
all individuals: 8638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41762
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2916
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2248
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.125199068969742e-5
allele num: 16326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -6.661e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

DP
type: SiteQuality
SIO_000300: 1.794667e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.03e-1

QD
type: SiteQuality
SIO_000300: 7.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

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

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

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 588
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
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: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.129704548240775e-5
allele num: 16314
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500780405811022e-5
allele num: 66632
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.357e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.95e0

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

DP
type: SiteQuality
SIO_000300: 1.794189e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

GenotypeQuality
all individuals: 8636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2909
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1988
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 815
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16310
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.742e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.421e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.793364e6

FS
type: SiteQuality
SIO_000300: 1.502e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.18e0

QD
type: SiteQuality
SIO_000300: 1.088e1

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8549
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2906
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41326
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16140
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503668952243474e-5
allele num: 66504
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.635e0

FS
type: SiteQuality
SIO_000300: 1.8525e1

DP
type: SiteQuality
SIO_000300: 1.785624e6

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.576e0

QD
type: SiteQuality
SIO_000300: 1.202e1

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

GenotypeQuality
all individuals: 8545
bin: 6.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41373
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503668952243474e-5
allele num: 66504
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16138
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.205e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

FS
type: SiteQuality
SIO_000300: 5.709e0

QD
type: SiteQuality
SIO_000300: 1.087e1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e-1

DP
type: SiteQuality
SIO_000300: 1.7854e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1957
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2893
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2206
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506069459923492e-5
allele num: 66398
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16084
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.756e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

DP
type: SiteQuality
SIO_000300: 1.781882e6

QD
type: SiteQuality
SIO_000300: 7.95e0

GenotypeQuality
all individuals: 1355
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 107
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2878
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 1954
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41169
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 806
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8449
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.012320390396723e-5
allele num: 66394
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16064
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.77e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.354e1

VQSLOD
type: SiteQuality
SIO_000300: 5.580000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.161e0

DP
type: SiteQuality
SIO_000300: 1.780205e6

GenotypeQuality
all individuals: 1332
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2866
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 38753
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1900
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8096
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65700
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.40450877417702e-5
allele num: 15614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.057e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-1

QD
type: SiteQuality
SIO_000300: 1.359e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 1.734926e6

GenotypeQuality
all individuals: 8084
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1329
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38869
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2863
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.044510747122937e-5
allele num: 65692
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15616
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.734486e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.808e0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.024e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

QD
type: SiteQuality
SIO_000300: 1.207e1

GenotypeQuality
all individuals: 2852
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3540
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1829
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2073
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1315
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7738
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528350909368791e-5
allele num: 65430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.705138e6

VQSLOD
type: SiteQuality
SIO_000300: 6.899999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.45e0

QD
type: SiteQuality
SIO_000300: 1.355e1

GenotypeQuality
all individuals: 1026
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5564
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3373
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2960
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4680
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 23439
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.931761343336905e-5
allele num: 11196
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63988
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.901960784313725e-4
allele num: 10200
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

FS
type: SiteQuality
SIO_000300: 8.65e-1

DP
type: SiteQuality
SIO_000300: 1.472574e6

QD
type: SiteQuality
SIO_000300: 1.63e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-2

GenotypeQuality
all individuals: 1447
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20357
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7980
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2805
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1705
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.570845114671693e-5
allele num: 63660
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14772
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

DP
type: SiteQuality
SIO_000300: 1.42225e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.09e-1

QD
type: SiteQuality
SIO_000300: 1.319e1

GenotypeQuality
all individuals: 704
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14902
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3660
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6583
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2818
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2511
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1169
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62974
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.241002730206007e-4
allele num: 8058
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11046
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.097e0

MQRankSum
type: SiteQuality
SIO_000300: -2.64e-1

DP
type: SiteQuality
SIO_000300: 1.359416e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.215e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-2

QD
type: SiteQuality
SIO_000300: 1.891e1

MQ
type: SiteQuality
SIO_000300: 5.75e1

GenotypeQuality
all individuals: 1536
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4307
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7239
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3995
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11479
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1578
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.604775812818949e-5
allele num: 62314
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.184e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.682e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.556e0

VQSLOD
type: SiteQuality
SIO_000300: 3.51e-1

DP
type: SiteQuality
SIO_000300: 1.335371e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

GenotypeQuality
all individuals: 1139
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3655
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5329
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2224
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2795
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5795
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3594
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2888
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.005025125628141e-4
allele num: 9950
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61032
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13610
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.189e0

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

MQ
type: SiteQuality
SIO_000300: 5.477e1

MQRankSum
type: SiteQuality
SIO_000300: -2.103e0

QD
type: SiteQuality
SIO_000300: 9.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

DP
type: SiteQuality
SIO_000300: 1.309952e6

GenotypeQuality
all individuals: 1872
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1862
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4088
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5732
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2669
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3544
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7698
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3053
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2229
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11126
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11078
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.21646831778707e-5
allele num: 62180
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.016e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

DP
type: SiteQuality
SIO_000300: 1.469551e6

FS
type: SiteQuality
SIO_000300: 2.894e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 589
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2791
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14834
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 928
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3002
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2083
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4569
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3882
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1747
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1532
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6110
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 10
allele frequency: 9.480470231323473e-4
allele num: 10548
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7938
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11136
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.76e0

DP
type: SiteQuality
SIO_000300: 1.492486e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

QD
type: SiteQuality
SIO_000300: 1.445e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 704
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1732
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4634
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6140
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2824
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1760
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3900
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7728
bin: 9.75e1
variant carriers: 1

Other
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: 11130
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.259763164525069e-4
allele num: 7938
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62352
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

MQRankSum
type: SiteQuality
SIO_000300: -6.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.824e0

VQSLOD
type: SiteQuality
SIO_000300: -7.805e-1

DP
type: SiteQuality
SIO_000300: 1.500712e6

QD
type: SiteQuality
SIO_000300: 8.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

GenotypeQuality
all individuals: 3997
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15843
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1684
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2690
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1492
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6216
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7936
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11138
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.010713563776026e-4
allele num: 9894
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62430
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.269e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.99e-1

DP
type: SiteQuality
SIO_000300: 1.512849e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.993e0

GenotypeQuality
all individuals: 2238
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4214
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6529
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3021
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10678
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.942944017170452e-5
allele num: 11182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7978
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.174e0

MQRankSum
type: SiteQuality
SIO_000300: -1.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.544009e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.149e0

QD
type: SiteQuality
SIO_000300: 9.58e0

GenotypeQuality
all individuals: 177
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3973
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2368
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22069
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4965
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3494
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3574
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8011
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1870
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.48714972641353e-4
allele num: 12062
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.66e-1

DP
type: SiteQuality
SIO_000300: 1.64427e6

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.28e1

MQ
type: SiteQuality
SIO_000300: 5.915e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

GenotypeQuality
all individuals: 5046
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3542
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8099
bin: 9.75e1
variant carriers: 40

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2423
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22553
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7821
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4053
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.539951573849879e-4
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.94811320754717e-4
allele num: 10176
num of homozygotes: 1

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

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 4.929143561306223e-4
allele num: 64920
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.588814744200826e-4
allele num: 12588
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.325581395348837e-3
allele num: 860
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.71e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.51e-1

DP
type: SiteQuality
SIO_000300: 1.66125e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.462e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.52e-1

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7989
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23630
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2475
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8147
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 318
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3636
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13842
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.771350400625366e-5
allele num: 10234
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.385e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e-1

DP
type: SiteQuality
SIO_000300: 1.685017e6

VQSLOD
type: SiteQuality
SIO_000300: 2.88e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.52e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e0

GenotypeQuality
all individuals: 8015
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23756
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2053
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3641
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8148
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4134
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2474
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65554
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.182876023559833e-5
allele num: 13922
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.912e1

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

VQSLOD
type: SiteQuality
SIO_000300: -3.673e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.64e-1

DP
type: SiteQuality
SIO_000300: 1.686971e6

QD
type: SiteQuality
SIO_000300: 1.695e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.465e0

FS
type: SiteQuality
SIO_000300: 2.103e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8037
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24075
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1933
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8159
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3651
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2485
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.042843232716651e-5
allele num: 65728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14328
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 3.511e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

QD
type: SiteQuality
SIO_000300: 1.444e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.693618e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.447e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.19e-1

GenotypeQuality
all individuals: 2497
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3688
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4183
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8150
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8169
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1938
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.032692424334324e-5
allele num: 65948
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14954
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.024e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

QD
type: SiteQuality
SIO_000300: 1.225e1

DP
type: SiteQuality
SIO_000300: 1.703576e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-1

FS
type: SiteQuality
SIO_000300: 4.113e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 3701
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24730
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8175
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5255
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4202
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2501
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 91
bin: 5.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514600751241973e-5
allele num: 66024
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.942879347192539e-4
allele num: 10294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15216
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.177e0

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

DP
type: SiteQuality
SIO_000300: 1.707723e6

FS
type: SiteQuality
SIO_000300: 2.721e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.081e1

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

GenotypeQuality
all individuals: 4247
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5296
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3746
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1958
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8200
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25096
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2516
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 10
allele frequency: 9.68804495252858e-4
allele num: 10322
num of homozygotes: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66290
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15722
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.41e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.71859e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.177e0

QD
type: SiteQuality
SIO_000300: 1.677e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 6.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

GenotypeQuality
all individuals: 8321
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4270
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5321
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3769
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 25211
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8239
bin: 9.75e1
variant carriers: 28

GenotypeQuality
all individuals: 588
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2526
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 8.180216461112509e-4
allele num: 15892
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.25998915205207e-4
allele num: 66372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

QD
type: SiteQuality
SIO_000300: 1.379e1

DP
type: SiteQuality
SIO_000300: 1.722644e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.03e-1

GenotypeQuality
all individuals: 3810
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25447
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2549
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8409
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5389
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4325
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503307276007216e-5
allele num: 66520
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: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 9.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.364e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

FS
type: SiteQuality
SIO_000300: 1.666e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.445e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 1.729886e6

GenotypeQuality
all individuals: 3826
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2007
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25519
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8449
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5426
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2560
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8255
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4350
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 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: 1
allele frequency: 6.090133982947625e-5
allele num: 16420
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.126e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.06e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.449e1

FS
type: SiteQuality
SIO_000300: 3.245e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.067e0

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e-1

DP
type: SiteQuality
SIO_000300: 1.733671e6

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

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8449
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2564
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3834
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25522
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8271
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 5423
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 8.75e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

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

Latino
type: Population
allele count: 4
allele frequency: 3.458412588621823e-4
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.050672430355427e-4
allele num: 66624
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.315e1

FS
type: SiteQuality
SIO_000300: 2.723e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.736645e6

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.231e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 2018
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3843
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2569
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8454
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25532
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5434
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4368
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.211e1

FS
type: SiteQuality
SIO_000300: 4.838e0

MQRankSum
type: SiteQuality
SIO_000300: 4.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.736992e6

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.74e-1

GenotypeQuality
all individuals: 25536
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4367
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2571
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2019
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5439
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3851
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8455
bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
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: 11564
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.228e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.313e0

MQRankSum
type: SiteQuality
SIO_000300: -5.04e-1

FS
type: SiteQuality
SIO_000300: 1.495e0

DP
type: SiteQuality
SIO_000300: 1.737415e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
all individuals: 2577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8465
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25561
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3855
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8286
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2020
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5449
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
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: 11572
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

QD
type: SiteQuality
SIO_000300: 1.324e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.55e-1

FS
type: SiteQuality
SIO_000300: 3.073e0

DP
type: SiteQuality
SIO_000300: 1.738604e6

MQ
type: SiteQuality
SIO_000300: 5.985e1

GenotypeQuality
all individuals: 47
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25562
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5451
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4378
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2021
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3857
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

QD
type: SiteQuality
SIO_000300: 1.806e1

DP
type: SiteQuality
SIO_000300: 1.739e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.905e0

MQ
type: SiteQuality
SIO_000300: 5.678e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

GenotypeQuality
all individuals: 2021
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4379
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5452
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3858
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8465
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8292
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.424e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.883e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.45e-1

DP
type: SiteQuality
SIO_000300: 1.739364e6

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.14e-1

FS
type: SiteQuality
SIO_000300: 1.966e0

VQSLOD
type: SiteQuality
SIO_000300: 8.92e-1

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8463
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5452
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25549
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4381
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2579
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8294
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3858
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 11572
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 6.504e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

QD
type: SiteQuality
SIO_000300: 1.499e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.436e0

VQSLOD
type: SiteQuality
SIO_000300: 6.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-1

DP
type: SiteQuality
SIO_000300: 1.739721e6

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8463
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5452
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2579
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8294
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 4381
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3858
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-1

FS
type: SiteQuality
SIO_000300: 6.504e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.739721e6

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.21e-1

QD
type: SiteQuality
SIO_000300: 1.499e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.436e0

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

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8305
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5453
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2582
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3865
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8491
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25551
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 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: 2
allele frequency: 2.997601918465228e-5
allele num: 66720
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.418e0

VQSLOD
type: SiteQuality
SIO_000300: 4.66e-1

DP
type: SiteQuality
SIO_000300: 1.741007e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.225e1

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

GenotypeQuality
all individuals: 3869
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5460
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2027
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25548
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2582
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8309
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8497
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

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

Latino
type: Population
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
allele num: 16510
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.55e-1

DP
type: SiteQuality
SIO_000300: 1.741415e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.43e-1

FS
type: SiteQuality
SIO_000300: 1.821e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.07e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.8e-1

QD
type: SiteQuality
SIO_000300: 1.163e1

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25539
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4388
bin: 8.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3867
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8489
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5459
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8333
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 1

Latino
type: Population
allele count: 22
allele frequency: 1.900155467265504e-3
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.86e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

DP
type: SiteQuality
SIO_000300: 1.745033e6

VQSLOD
type: SiteQuality
SIO_000300: 5.27e0

QD
type: SiteQuality
SIO_000300: 1.418e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.67e-1

GenotypeQuality
all individuals: 8335
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2580
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8493
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5465
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 25535
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3870
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.9e-2

DP
type: SiteQuality
SIO_000300: 1.743774e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.206e0

QD
type: SiteQuality
SIO_000300: 1.175e1

MQRankSum
type: SiteQuality
SIO_000300: 2.66e-1

FS
type: SiteQuality
SIO_000300: 8.25e-1

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

GenotypeQuality
all individuals: 5465
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25543
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8335
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3870
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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

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

MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
SIO_000300: 1.246e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.64e-1

DP
type: SiteQuality
SIO_000300: 1.743673e6

FS
type: SiteQuality
SIO_000300: 6.105e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.154e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

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

GenotypeQuality
all individuals: 8336
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 25544
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3871
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4388
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2580
bin: 9.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 8492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5464
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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

FS
type: SiteQuality
SIO_000300: 1.107e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.743984e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.132e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e0

QD
type: SiteQuality
SIO_000300: 1.281e1

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8493
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3870
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8337
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25542
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4388
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5464
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -8.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.99e1

DP
type: SiteQuality
SIO_000300: 1.744088e6

FS
type: SiteQuality
SIO_000300: 3.68e-1

QD
type: SiteQuality
SIO_000300: 1.295e1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2580
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8337
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3870
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25542
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8493
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5464
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4388
bin: 8.25e1
variant carriers: 0

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

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

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: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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

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

MQ
type: SiteQuality
SIO_000300: 5.99e1

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-2

FS
type: SiteQuality
SIO_000300: 3.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.295e1

DP
type: SiteQuality
SIO_000300: 1.744088e6

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

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8494
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5464
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8338
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 3872
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25543
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4388
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2579
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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

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

DP
type: SiteQuality
SIO_000300: 1.744151e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.77e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.84e-1

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeQuality
all individuals: 5463
bin: 7.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8495
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8344
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3870
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25535
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

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

Latino
type: Population
allele count: 6
allele frequency: 5.182242183451373e-4
allele num: 11578
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.703e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.294e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 1.745019e6

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5464
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2581
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8349
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 3871
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
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: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.396e0

QD
type: SiteQuality
SIO_000300: 1.312e1

DP
type: SiteQuality
SIO_000300: 1.745324e6

MQRankSum
type: SiteQuality
SIO_000300: 7.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 4.099e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

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

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

GenotypeQuality
all individuals: 8349
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 8495
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25526
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3872
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5464
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2581
bin: 9.25e1
variant carriers: 0

Latino
type: Population
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
allele num: 16512
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

FS
type: SiteQuality
SIO_000300: 3.456e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.89e0

DP
type: SiteQuality
SIO_000300: 1.745093e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.161e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e-1

GenotypeQuality
all individuals: 3872
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 25525
bin: 6.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 5463
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8494
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8350
bin: 9.75e1
variant carriers: 1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.079e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.396e1

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.403e0

DP
type: SiteQuality
SIO_000300: 1.745153e6

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2579
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4390
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3873
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8351
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25524
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5464
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e-1

QD
type: SiteQuality
SIO_000300: 1.389e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.533e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.91e0

DP
type: SiteQuality
SIO_000300: 1.745247e6

FS
type: SiteQuality
SIO_000300: 5.580000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

GenotypeQuality
all individuals: 4390
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8355
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1
bin: 3.25e1
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: 3873
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25521
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2579
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5463
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8494
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.25e-1

DP
type: SiteQuality
SIO_000300: 1.745656e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.107e0

VQSLOD
type: SiteQuality
SIO_000300: -6.187e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 9.962e0

QD
type: SiteQuality
SIO_000300: 1.349e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.27e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

GenotypeQuality
all individuals: 3873
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4391
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2580
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5463
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25517
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8356
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.28e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.254e1

FS
type: SiteQuality
SIO_000300: 3.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.100000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.745496e6

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.46e-1

GenotypeDepth
all individuals: 150
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 8493
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25503
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5465
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3872
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8357
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2580
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 66736
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.62e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

QD
type: SiteQuality
SIO_000300: 1.24e1

FS
type: SiteQuality
SIO_000300: 1.483e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.217e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.09e0

MQRankSum
type: SiteQuality
SIO_000300: -1.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

DP
type: SiteQuality
SIO_000300: 1.745446e6

GenotypeQuality
all individuals: 2580
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8494
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5465
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8358
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25459
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3872
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.296e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

FS
type: SiteQuality
SIO_000300: 1.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-2

DP
type: SiteQuality
SIO_000300: 1.745105e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.88e-1

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

GenotypeQuality
all individuals: 4389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25452
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5463
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2579
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3869
bin: 7.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 6
allele frequency: 5.768121515093252e-4
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.993e0

VQSLOD
type: SiteQuality
SIO_000300: 2.15e0

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-2

DP
type: SiteQuality
SIO_000300: 1.745607e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.391e0

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

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

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4388
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8481
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2579
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5463
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25354
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8364
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

QD
type: SiteQuality
SIO_000300: 1.338e1

MQ
type: SiteQuality
SIO_000300: 5.988e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e0

DP
type: SiteQuality
SIO_000300: 1.744429e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

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

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5460
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3871
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 8469
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25198
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 9.76e0

VQSLOD
type: SiteQuality
SIO_000300: -3.5e-1

DP
type: SiteQuality
SIO_000300: 1.742707e6

FS
type: SiteQuality
SIO_000300: 2.367e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 8469
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8366
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 25198
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5460
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4388
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3871
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 9.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.29e-1

FS
type: SiteQuality
SIO_000300: 2.367e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

DP
type: SiteQuality
SIO_000300: 1.742707e6

VQSLOD
type: SiteQuality
SIO_000300: -3.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 5460
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25135
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8456
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3870
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8377
bin: 9.75e1
variant carriers: 13

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

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

African
type: Population
allele count: 12
allele frequency: 1.15473441108545e-3
allele num: 10392
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.593e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.635e0

QD
type: SiteQuality
SIO_000300: 1.336e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

DP
type: SiteQuality
SIO_000300: 1.743148e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

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

GenotypeQuality
all individuals: 2576
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3870
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 101
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4387
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5458
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25027
bin: 6.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
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: 908
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.48e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

FS
type: SiteQuality
SIO_000300: 3.613e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.215e1

DP
type: SiteQuality
SIO_000300: 1.742484e6

MQ
type: SiteQuality
SIO_000300: 5.939e1

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.562e0

GenotypeQuality
all individuals: 8443
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 24976
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5459
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2578
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3867
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4385
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8383
bin: 9.75e1
variant carriers: 3

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.470615455807496e-4
allele num: 8644
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -4.686e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.346e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

DP
type: SiteQuality
SIO_000300: 1.742458e6

QD
type: SiteQuality
SIO_000300: 1.623e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.978e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.143e0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5462
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3865
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24907
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8385
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8443
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.470615455807496e-4
allele num: 8644
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.89e-1

FS
type: SiteQuality
SIO_000300: 5.301e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.671e0

DP
type: SiteQuality
SIO_000300: 1.742567e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.495e1

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.37e-1