19-11664752-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664752
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664752
    reference: chr 19
allele count: 3
allele frequency: 2.476514388548598e-5
allele num: 121138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.261A>G
  hgvsp: ENST00000591912.1:c.261A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.187+74A>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.187+74A>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.187+74A>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.187+74A>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.250+74A>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.208+74A>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.187+74A>G
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15438
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15434
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro87Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

19-11664762-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664762
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664762
    reference: chr 19
allele count: 10
allele frequency: 8.252867871585376e-5
allele num: 121170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.187+64C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.187+64C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.187+64C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.187+64C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.251C>A
  hgvsp: ENSP00000466665.1:p.Ser84Ter
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.208+64C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.187+64C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.250+64C>A
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4835
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7805
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser84Ter
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

19-11664768-GGTCCGGACTCCAGCCCC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664768
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664751
    reference: chr 19
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsp: ENSP00000466665.1:p.Arg76SerfsTer24
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3417
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg76SerfsTer24
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: GGTCCGGACTCCAGCCCC
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

19-11664769-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664769
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664769
    reference: chr 19
allele count: 4
allele frequency: 3.30011220381493e-5
allele num: 121208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.187+57C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.187+57C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.244C>T
  hgvsp: ENSP00000466665.1:p.Pro82Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.208+57C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.187+57C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.187+57C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.250+57C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.187+57C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4804
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15404
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4469
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro82Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-11664769-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664769
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664769
    reference: chr 19
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.250+57C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.187+57C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.187+57C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.187+57C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.208+57C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.187+57C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.187+57C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.244C>A
  hgvsp: ENSP00000466665.1:p.Pro82Thr
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7808
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15475
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4469
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro82Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

19-11664772-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664772
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664772
    reference: chr 19
allele count: 5
allele frequency: 4.125004125004125e-5
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.208+54G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.241G>A
  hgvsp: ENSP00000466665.1:p.Gly81Arg
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.187+54G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.250+54G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.187+54G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.187+54G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.187+54G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.187+54G>A
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5837
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15381
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15481
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 7798
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly81Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

19-11664773-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664773
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664773
    reference: chr 19
allele count: 3
allele frequency: 2.474594166556685e-5
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.208+53C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.187+53C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.187+53C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.187+53C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.187+53C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.187+53C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.240C>T
  hgvsp: ENST00000591912.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.250+53C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser80Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-11664776-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664776
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664776
    reference: chr 19
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.187+50G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.187+50G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.208+50G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.237G>A
  hgvsp: ENST00000591912.1:c.237G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.187+50G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.250+50G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.187+50G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.187+50G>A
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7815
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5839
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu79Glu
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

19-11664781-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664781
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664780
    reference: chr 19
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.187+44delG
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.187+44delG
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.208+44delG
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.187+44delG
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.250+44delG
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.187+44delG
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.187+44delG
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.231delG
  hgvsp: ENSP00000466665.1:p.Leu78TrpfsTer33
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15496
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15482
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu78TrpfsTer33
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: GC
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum

http://identifiers.org/exac.variant/19-11664782-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664782
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664782
    reference: chr 19
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.231G>T
  hgvsp: ENST00000591912.1:c.231G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.187+44G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.250+44G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.187+44G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.187+44G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.187+44G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.187+44G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.208+44G>T
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7819
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3428
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4821
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly77Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

19-11664792-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664792
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664792
    reference: chr 19
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.187+34T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.208+34T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.187+34T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.221T>C
  hgvsp: ENSP00000466665.1:p.Val74Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.187+34T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.250+34T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.187+34T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.187+34T>C
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5840
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val74Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-11664810-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664810
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664810
    reference: chr 19
allele count: 6
allele frequency: 4.945435363159804e-5
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.187+16T>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.208+16T>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.187+16T>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.203T>G
  hgvsp: ENSP00000466665.1:p.Leu68Arg
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.187+16T>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.187+16T>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.250+16T>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.187+16T>G
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14951
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3438
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15675
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2677
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4516
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu68Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

19-11664827-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664827
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664827
    reference: chr 19
allele count: 2
allele frequency: 1.648098094798602e-5
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.186G>A
  hgvsp: ENST00000589171.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.186G>A
  hgvsp: ENST00000252445.3:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.186G>A
  hgvsp: ENST00000590700.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.186G>A
  hgvsp: ENST00000586683.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.186G>A
  hgvsp: ENST00000591912.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.249G>A
  hgvsp: ENST00000587806.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.207G>A
  hgvsp: ENST00000591674.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.186G>A
  hgvsp: ENST00000586120.1:c.186G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4523
  bin: 7.25e1
  variant carriers: 0
hgvs: c.186G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

19-11664832-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664832
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664832
    reference: chr 19
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.181A>G
  hgvsp: ENSP00000467914.1:p.Ile61Val
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.181A>G
  hgvsp: ENSP00000252445.3:p.Ile61Val
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.181A>G
  hgvsp: ENSP00000467264.1:p.Ile61Val
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.181A>G
  hgvsp: ENSP00000466732.1:p.Ile61Val
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.244A>G
  hgvsp: ENSP00000465765.1:p.Ile82Val
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.181A>G
  hgvsp: ENSP00000467664.1:p.Ile61Val
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.202A>G
  hgvsp: ENSP00000467330.1:p.Ile68Val
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.181A>G
  hgvsp: ENSP00000466665.1:p.Ile61Val
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15511
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile61Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

19-11664836-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664836
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664836
    reference: chr 19
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.177G>A
  hgvsp: ENST00000586683.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.177G>A
  hgvsp: ENST00000586120.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.177G>A
  hgvsp: ENST00000589171.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.177G>A
  hgvsp: ENST00000590700.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.177G>A
  hgvsp: ENST00000252445.3:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.177G>A
  hgvsp: ENST00000591912.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.198G>A
  hgvsp: ENST00000591674.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.240G>A
  hgvsp: ENST00000587806.1:c.240G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4851
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15792
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7916
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr59Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

19-11664837-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664837
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664837
    reference: chr 19
allele count: 2
allele frequency: 1.647880825258717e-5
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.176C>T
  hgvsp: ENSP00000467264.1:p.Thr59Met
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.176C>T
  hgvsp: ENSP00000467914.1:p.Thr59Met
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.176C>T
  hgvsp: ENSP00000466732.1:p.Thr59Met
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.239C>T
  hgvsp: ENSP00000465765.1:p.Thr80Met
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.176C>T
  hgvsp: ENSP00000252445.3:p.Thr59Met
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.176C>T
  hgvsp: ENSP00000467664.1:p.Thr59Met
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.197C>T
  hgvsp: ENSP00000467330.1:p.Thr66Met
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.176C>T
  hgvsp: ENSP00000466665.1:p.Thr59Met
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  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
genotype quality: GenotypeQuality
  all individuals: 4852
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr59Met
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-11664847-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664847
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664847
    reference: chr 19
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.166G>A
  hgvsp: ENSP00000466732.1:p.Glu56Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.166G>A
  hgvsp: ENSP00000466665.1:p.Glu56Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.229G>A
  hgvsp: ENSP00000465765.1:p.Glu77Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.166G>A
  hgvsp: ENSP00000467264.1:p.Glu56Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.166G>A
  hgvsp: ENSP00000467664.1:p.Glu56Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.166G>A
  hgvsp: ENSP00000467914.1:p.Glu56Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.166G>A
  hgvsp: ENSP00000252445.3:p.Glu56Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.187G>A
  hgvsp: ENSP00000467330.1:p.Glu63Lys
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4858
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7924
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3439
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu56Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/19-11664855-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664855
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664855
    reference: chr 19
allele count: 2
allele frequency: 1.647690761397901e-5
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.221G>T
  hgvsp: ENSP00000465765.1:p.Cys74Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.158G>T
  hgvsp: ENSP00000467914.1:p.Cys53Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.158G>T
  hgvsp: ENSP00000467664.1:p.Cys53Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.179G>T
  hgvsp: ENSP00000467330.1:p.Cys60Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.158G>T
  hgvsp: ENSP00000466665.1:p.Cys53Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.158G>T
  hgvsp: ENSP00000466732.1:p.Cys53Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.158G>T
  hgvsp: ENSP00000252445.3:p.Cys53Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.158G>T
  hgvsp: ENSP00000467264.1:p.Cys53Phe
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4528
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5880
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys53Phe
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

19-11664857-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664857
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664857
    reference: chr 19
allele count: 15
allele frequency: 1.235768071048426e-4
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.156G>A
  hgvsp: ENST00000252445.3:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.156G>A
  hgvsp: ENST00000586683.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.219G>A
  hgvsp: ENST00000587806.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.156G>A
  hgvsp: ENST00000586120.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.156G>A
  hgvsp: ENST00000591912.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.156G>A
  hgvsp: ENST00000590700.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.156G>A
  hgvsp: ENST00000589171.1:c.156G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.177G>A
  hgvsp: ENST00000591674.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5882
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2681
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val52Val
num of homozygotes: 1
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

19-11664862-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664862
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664862
    reference: chr 19
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.172A>G
  hgvsp: ENSP00000467330.1:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.151A>G
  hgvsp: ENSP00000466732.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.214A>G
  hgvsp: ENSP00000465765.1:p.Thr72Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.151A>G
  hgvsp: ENSP00000467664.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.151A>G
  hgvsp: ENSP00000467264.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.151A>G
  hgvsp: ENSP00000466665.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.151A>G
  hgvsp: ENSP00000252445.3:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.151A>G
  hgvsp: ENSP00000467914.1:p.Thr51Ala
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12684
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13068
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3438
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5885
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr51Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

19-11664863-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664863
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664863
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.150T>C
  hgvsp: ENST00000589171.1:c.150T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.171T>C
  hgvsp: ENST00000591674.1:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.150T>C
  hgvsp: ENST00000252445.3:c.150T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.150T>C
  hgvsp: ENST00000586683.1:c.150T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.150T>C
  hgvsp: ENST00000586120.1:c.150T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.213T>C
  hgvsp: ENST00000587806.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.150T>C
  hgvsp: ENST00000590700.1:c.150T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.150T>C
  hgvsp: ENST00000591912.1:c.150T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4530
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Cys50Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-11664866-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664866
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664866
    reference: chr 19
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.168T>G
  hgvsp: ENST00000591674.1:c.168T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.147T>G
  hgvsp: ENST00000586683.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.147T>G
  hgvsp: ENST00000252445.3:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.147T>G
  hgvsp: ENST00000586120.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.210T>G
  hgvsp: ENST00000587806.1:c.210T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.147T>G
  hgvsp: ENST00000591912.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.147T>G
  hgvsp: ENST00000589171.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.147T>G
  hgvsp: ENST00000590700.1:c.147T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2684
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7929
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser49Ser
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-11664877-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664877
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664877
    reference: chr 19
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.136G>A
  hgvsp: ENSP00000466665.1:p.Gly46Arg
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.136G>A
  hgvsp: ENSP00000466732.1:p.Gly46Arg
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.136G>A
  hgvsp: ENSP00000252445.3:p.Gly46Arg
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.136G>A
  hgvsp: ENSP00000467664.1:p.Gly46Arg
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.136G>A
  hgvsp: ENSP00000467264.1:p.Gly46Arg
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.199G>A
  hgvsp: ENSP00000465765.1:p.Gly67Arg
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.157G>A
  hgvsp: ENSP00000467330.1:p.Gly53Arg
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.136G>A
  hgvsp: ENSP00000467914.1:p.Gly46Arg
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7937
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4536
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15530
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly46Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-11664878-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664878
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664878
    reference: chr 19
allele count: 6
allele frequency: 4.94274651948266e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.198C>T
  hgvsp: ENST00000587806.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.135C>T
  hgvsp: ENST00000590700.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.135C>T
  hgvsp: ENST00000252445.3:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.135C>T
  hgvsp: ENST00000586683.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.156C>T
  hgvsp: ENST00000591674.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.135C>T
  hgvsp: ENST00000591912.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.135C>T
  hgvsp: ENST00000589171.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.135C>T
  hgvsp: ENST00000586120.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4536
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4862
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr45Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum

19-11664884-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664884
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664884
    reference: chr 19
allele count: 10
allele frequency: 8.237910865804432e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.150C>T
  hgvsp: ENST00000591674.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.129C>T
  hgvsp: ENST00000252445.3:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.192C>T
  hgvsp: ENST00000587806.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.129C>T
  hgvsp: ENST00000586120.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.129C>T
  hgvsp: ENST00000586683.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.129C>T
  hgvsp: ENST00000591912.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.129C>T
  hgvsp: ENST00000589171.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.129C>T
  hgvsp: ENST00000590700.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15773
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4536
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg43Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

19-11664885-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664885
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664885
    reference: chr 19
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.128G>A
  hgvsp: ENSP00000467264.1:p.Arg43His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.128G>A
  hgvsp: ENSP00000467664.1:p.Arg43His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.128G>A
  hgvsp: ENSP00000252445.3:p.Arg43His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.128G>A
  hgvsp: ENSP00000466665.1:p.Arg43His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.128G>A
  hgvsp: ENSP00000467914.1:p.Arg43His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.149G>A
  hgvsp: ENSP00000467330.1:p.Arg50His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.128G>A
  hgvsp: ENSP00000466732.1:p.Arg43His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.191G>A
  hgvsp: ENSP00000465765.1:p.Arg64His
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15773
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4537
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4863
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2684
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg43His
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

19-11664886-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664886
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664886
    reference: chr 19
allele count: 4
allele frequency: 3.295164346321773e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.127C>T
  hgvsp: ENSP00000467664.1:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.190C>T
  hgvsp: ENSP00000465765.1:p.Arg64Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.127C>T
  hgvsp: ENSP00000252445.3:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.148C>T
  hgvsp: ENSP00000467330.1:p.Arg50Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.127C>T
  hgvsp: ENSP00000467914.1:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.127C>T
  hgvsp: ENSP00000466732.1:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.127C>T
  hgvsp: ENSP00000467264.1:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.127C>T
  hgvsp: ENSP00000466665.1:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5885
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15771
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg43Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

19-11664892-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664892
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664892
    reference: chr 19
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.121C>T
  hgvsp: ENSP00000467264.1:p.Arg41Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.121C>T
  hgvsp: ENSP00000467914.1:p.Arg41Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.184C>T
  hgvsp: ENSP00000465765.1:p.Arg62Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.121C>T
  hgvsp: ENSP00000466665.1:p.Arg41Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.142C>T
  hgvsp: ENSP00000467330.1:p.Arg48Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.121C>T
  hgvsp: ENSP00000466732.1:p.Arg41Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.121C>T
  hgvsp: ENSP00000252445.3:p.Arg41Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.121C>T
  hgvsp: ENSP00000467664.1:p.Arg41Cys
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg41Cys
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-11664907-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664907
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664907
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.117-11G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.180-11G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.117-11G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.117-11G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.117-11G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.117-11G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.138-11G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.117-11G>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2684
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15769
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD

19-11664911-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664911
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664911
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.180-15C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.138-15C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.117-15C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.117-15C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.117-15C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.117-15C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.117-15C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.117-15C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 1
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: 4863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4867
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

19-11664916-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664916
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664916
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.117-20C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.117-20C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.117-20C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.117-20C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.138-20C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.180-20C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.117-20C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.117-20C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15553
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS

19-11664918-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664918
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664918
    reference: chr 19
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.138-22C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.117-22C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.117-22C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.117-22C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.117-22C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.117-22C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.117-22C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.180-22C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 4.25e1
  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: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15759
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7934
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-11664922-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664922
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664922
    reference: chr 19
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.117-26C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.117-26C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.180-26C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.117-26C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.138-26C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.117-26C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.117-26C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.117-26C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5894
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7935
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

19-11664929-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664929
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664929
    reference: chr 19
allele count: 32
allele frequency: 2.635740643120717e-4
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.138-33T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.117-33T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.180-33T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.117-33T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.117-33T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.117-33T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.117-33T>C
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.117-33T>C
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12693
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4539
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7936
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 1
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

19-11664938-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664938
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664938
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.117-42A>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.117-42A>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.180-42A>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.117-42A>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.117-42A>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.117-42A>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.117-42A>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.138-42A>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7931
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4543
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

19-11664943-CTGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664943
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664940
    reference: chr 19
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.180-50_180-48delACA
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.117-50_117-48delACA
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.117-50_117-48delACA
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.117-50_117-48delACA
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.117-50_117-48delACA
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.138-50_138-48delACA
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.117-50_117-48delACA
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.117-50_117-48delACA
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15603
  bin: 6.25e1
  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: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: CTGT
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

19-11664947-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664947
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664947
    reference: chr 19
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.117-51C>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.138-51C>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.117-51C>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.117-51C>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.117-51C>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.117-51C>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.117-51C>G
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.180-51C>G
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4534
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5896
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15503
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-11664996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664996
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664996
    reference: chr 19
allele count: 68
allele frequency: 5.604272433572888e-4
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+51G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+51G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+51G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+51G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+51G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+51G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+51G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+51G>A
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 24064
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16689
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7710
  bin: 9.75e1
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

19-11664997-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664997
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664997
    reference: chr 19
allele count: 3
allele frequency: 2.472147142197904e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+50C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+50C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+50C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+50C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+50C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+50C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+50C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+50C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9207
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31855
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7640
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

19-11664998-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664998
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664998
    reference: chr 19
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+49C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+49C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+49C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+49C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+49C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+49C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+49C>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+49C>A
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9209
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2946
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

19-11664999-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11664999
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11664999
    reference: chr 19
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+48C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+48C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+48C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+48C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+48C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+48C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+48C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+48C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2950
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9198
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

19-11665003-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665003
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665003
    reference: chr 19
allele count: 29
allele frequency: 2.389781623403379e-4
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+44C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+44C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+44C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+44C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+44C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+44C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+44C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+44C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24135
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16660
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 986
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31876
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

19-11665011-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665011
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665011
    reference: chr 19
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+36C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+36C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+36C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+36C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+36C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+36C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+36C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+36C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2446
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3774
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum

19-11665013-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665013
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665013
    reference: chr 19
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+34C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+34C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+34C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+34C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+34C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+34C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+34C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+34C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3763
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9140
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2912
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
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: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-11665016-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665016
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665016
    reference: chr 19
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+31C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+31C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+31C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+31C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+31C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+31C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+31C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+31C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7589
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9122
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2910
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum

19-11665020-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665020
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665020
    reference: chr 19
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+27C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+27C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+27C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+27C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+27C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+27C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+27C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+27C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3745
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9096
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31907
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 964
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

19-11665031-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665031
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665031
    reference: chr 19
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+16G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+16G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+16G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+16G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+16G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+16G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+16G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+16G>A
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3718
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7573
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

19-11665039-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665039
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665039
    reference: chr 19
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+8G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+8G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+8G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+8G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+8G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+8G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+8G>A
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+8G>A
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8991
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
hgvs: c.116+8G>A
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/19-11665040-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665040
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665040
    reference: chr 19
allele count: 7
allele frequency: 5.770435585451908e-5
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.116+7G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.116+7G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.137+7G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.116+7G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.116+7G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.116+7G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.116+7G>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.179+7G>T
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16420
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7568
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 7.25e1
  variant carriers: 0
hgvs: c.116+7G>T
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

19-11665055-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665055
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665055
    reference: chr 19
allele count: 3
allele frequency: 2.472636159831201e-5
allele num: 121328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.108T>C
  hgvsp: ENST00000586683.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.108T>C
  hgvsp: ENST00000252445.3:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.129T>C
  hgvsp: ENST00000591674.1:c.129T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.108T>C
  hgvsp: ENST00000586120.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.108T>C
  hgvsp: ENST00000589171.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.108T>C
  hgvsp: ENST00000591912.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.108T>C
  hgvsp: ENST00000590700.1:c.108T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.171T>C
  hgvsp: ENST00000587806.1:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24170
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3694
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2411
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp36Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

19-11665060-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665060
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665060
    reference: chr 19
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.103T>A
  hgvsp: ENSP00000466732.1:p.Cys35Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.103T>A
  hgvsp: ENSP00000252445.3:p.Cys35Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.166T>A
  hgvsp: ENSP00000465765.1:p.Cys56Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.103T>A
  hgvsp: ENSP00000466665.1:p.Cys35Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.103T>A
  hgvsp: ENSP00000467664.1:p.Cys35Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.103T>A
  hgvsp: ENSP00000467914.1:p.Cys35Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.124T>A
  hgvsp: ENSP00000467330.1:p.Cys42Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.103T>A
  hgvsp: ENSP00000467264.1:p.Cys35Ser
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24209
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7557
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Cys35Ser
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

19-11665062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665062
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665062
    reference: chr 19
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.101C>T
  hgvsp: ENSP00000467264.1:p.Ser34Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.101C>T
  hgvsp: ENSP00000466732.1:p.Ser34Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.101C>T
  hgvsp: ENSP00000466665.1:p.Ser34Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.101C>T
  hgvsp: ENSP00000467664.1:p.Ser34Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.164C>T
  hgvsp: ENSP00000465765.1:p.Ser55Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.122C>T
  hgvsp: ENSP00000467330.1:p.Ser41Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.101C>T
  hgvsp: ENSP00000252445.3:p.Ser34Phe
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.101C>T
  hgvsp: ENSP00000467914.1:p.Ser34Phe
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser34Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

19-11665067-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665067
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665067
    reference: chr 19
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.96G>A
  hgvsp: ENST00000586120.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.159G>A
  hgvsp: ENST00000587806.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.96G>A
  hgvsp: ENST00000590700.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.96G>A
  hgvsp: ENST00000252445.3:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.96G>A
  hgvsp: ENST00000589171.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.117G>A
  hgvsp: ENST00000591674.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.96G>A
  hgvsp: ENST00000586683.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.96G>A
  hgvsp: ENST00000591912.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16398
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu32Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

19-11665070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665070
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665070
    reference: chr 19
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.93C>T
  hgvsp: ENST00000589171.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.93C>T
  hgvsp: ENST00000586120.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.93C>T
  hgvsp: ENST00000590700.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.114C>T
  hgvsp: ENST00000591674.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.93C>T
  hgvsp: ENST00000252445.3:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.93C>T
  hgvsp: ENST00000586683.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.93C>T
  hgvsp: ENST00000591912.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.156C>T
  hgvsp: ENST00000587806.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2827
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3685
  bin: 7.75e1
  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: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His31His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

19-11665094-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665094
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665094
    reference: chr 19
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.69G>A
  hgvsp: ENST00000586120.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.69G>A
  hgvsp: ENST00000589171.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.69G>A
  hgvsp: ENST00000590700.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.69G>A
  hgvsp: ENST00000591912.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.132G>A
  hgvsp: ENST00000587806.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.69G>A
  hgvsp: ENST00000586683.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.90G>A
  hgvsp: ENST00000591674.1:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.69G>A
  hgvsp: ENST00000252445.3:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln23Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-11665102-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665102
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665102
    reference: chr 19
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.61G>A
  hgvsp: ENSP00000466732.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.61G>A
  hgvsp: ENSP00000467264.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.124G>A
  hgvsp: ENSP00000465765.1:p.Glu42Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.61G>A
  hgvsp: ENSP00000467914.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.61G>A
  hgvsp: ENSP00000466665.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.61G>A
  hgvsp: ENSP00000467664.1:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.82G>A
  hgvsp: ENSP00000467330.1:p.Glu28Lys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.61G>A
  hgvsp: ENSP00000252445.3:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32813
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3682
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8995
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu21Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD

19-11665103-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665103
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665103
    reference: chr 19
allele count: 5
allele frequency: 4.120381052839767e-5
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.60C>T
  hgvsp: ENST00000589171.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.60C>T
  hgvsp: ENST00000591912.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.60C>T
  hgvsp: ENST00000586120.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.81C>T
  hgvsp: ENST00000591674.1:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.60C>T
  hgvsp: ENST00000590700.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.60C>T
  hgvsp: ENST00000252445.3:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.123C>T
  hgvsp: ENST00000587806.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.60C>T
  hgvsp: ENST00000586683.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu20Leu
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: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

19-11665103-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665103
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665103
    reference: chr 19
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.60C>G
  hgvsp: ENST00000252445.3:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.60C>G
  hgvsp: ENST00000591912.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.60C>G
  hgvsp: ENST00000590700.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.81C>G
  hgvsp: ENST00000591674.1:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.60C>G
  hgvsp: ENST00000589171.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.60C>G
  hgvsp: ENST00000586683.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.60C>G
  hgvsp: ENST00000586120.1:c.60C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.123C>G
  hgvsp: ENST00000587806.1:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32819
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8998
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2823
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3682
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu20Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD

19-11665108-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665108
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665108
    reference: chr 19
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.55A>G
  hgvsp: ENSP00000252445.3:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.55A>G
  hgvsp: ENSP00000466665.1:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.55A>G
  hgvsp: ENSP00000467264.1:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.76A>G
  hgvsp: ENSP00000467330.1:p.Thr26Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.118A>G
  hgvsp: ENSP00000465765.1:p.Thr40Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.55A>G
  hgvsp: ENSP00000467914.1:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.55A>G
  hgvsp: ENSP00000467664.1:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.55A>G
  hgvsp: ENSP00000466732.1:p.Thr19Ala
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8999
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3683
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr19Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

19-11665120-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665120
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665120
    reference: chr 19
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.106A>G
  hgvsp: ENSP00000465765.1:p.Lys36Glu
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.43A>G
  hgvsp: ENSP00000466732.1:p.Lys15Glu
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.43A>G
  hgvsp: ENSP00000467664.1:p.Lys15Glu
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.43A>G
  hgvsp: ENSP00000467914.1:p.Lys15Glu
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.43A>G
  hgvsp: ENSP00000467264.1:p.Lys15Glu
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.43A>G
  hgvsp: ENSP00000252445.3:p.Lys15Glu
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.43A>G
  hgvsp: ENSP00000466665.1:p.Lys15Glu
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.64A>G
  hgvsp: ENSP00000467330.1:p.Lys22Glu
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8996
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7546
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2824
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys15Glu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

19-11665126-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665126
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665126
    reference: chr 19
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.58A>C
  hgvsp: ENSP00000467330.1:p.Lys20Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.37A>C
  hgvsp: ENSP00000467664.1:p.Lys13Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.100A>C
  hgvsp: ENSP00000465765.1:p.Lys34Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.37A>C
  hgvsp: ENSP00000466665.1:p.Lys13Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.37A>C
  hgvsp: ENSP00000467914.1:p.Lys13Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.37A>C
  hgvsp: ENSP00000466732.1:p.Lys13Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.37A>C
  hgvsp: ENSP00000252445.3:p.Lys13Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.37A>C
  hgvsp: ENSP00000467264.1:p.Lys13Gln
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32799
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys13Gln
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ

19-11665127-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665127
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665127
    reference: chr 19
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.36C>T
  hgvsp: ENST00000591912.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.36C>T
  hgvsp: ENST00000590700.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.36C>T
  hgvsp: ENST00000586120.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.36C>T
  hgvsp: ENST00000586683.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.36C>T
  hgvsp: ENST00000252445.3:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.57C>T
  hgvsp: ENST00000591674.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.36C>T
  hgvsp: ENST00000589171.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.99C>T
  hgvsp: ENST00000587806.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8994
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro12Pro
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/19-11665130-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665130
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665130
    reference: chr 19
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.96T>G
  hgvsp: ENST00000587806.1:c.96T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.33T>G
  hgvsp: ENST00000252445.3:c.33T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.33T>G
  hgvsp: ENST00000589171.1:c.33T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.33T>G
  hgvsp: ENST00000586683.1:c.33T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.33T>G
  hgvsp: ENST00000586120.1:c.33T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.54T>G
  hgvsp: ENST00000591674.1:c.54T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.33T>G
  hgvsp: ENST00000591912.1:c.33T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.33T>G
  hgvsp: ENST00000590700.1:c.33T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro11Pro
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-11665132-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665132
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665132
    reference: chr 19
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.31C>T
  hgvsp: ENSP00000466732.1:p.Pro11Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.31C>T
  hgvsp: ENSP00000467664.1:p.Pro11Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.31C>T
  hgvsp: ENSP00000252445.3:p.Pro11Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.31C>T
  hgvsp: ENSP00000467264.1:p.Pro11Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.52C>T
  hgvsp: ENSP00000467330.1:p.Pro18Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.31C>T
  hgvsp: ENSP00000467914.1:p.Pro11Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.94C>T
  hgvsp: ENSP00000465765.1:p.Pro32Ser
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.31C>T
  hgvsp: ENSP00000466665.1:p.Pro11Ser
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro11Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS

19-11665133-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665133
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665133
    reference: chr 19
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.30G>C
  hgvsp: ENST00000252445.3:c.30G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.30G>C
  hgvsp: ENST00000590700.1:c.30G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.30G>C
  hgvsp: ENST00000589171.1:c.30G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.30G>C
  hgvsp: ENST00000586120.1:c.30G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.30G>C
  hgvsp: ENST00000591912.1:c.30G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.93G>C
  hgvsp: ENST00000587806.1:c.93G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.30G>C
  hgvsp: ENST00000586683.1:c.30G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.51G>C
  hgvsp: ENST00000591674.1:c.51G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro10Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

19-11665133-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665133
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665133
    reference: chr 19
allele count: 3
allele frequency: 2.473329266080762e-5
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.30G>A
  hgvsp: ENST00000586120.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.51G>A
  hgvsp: ENST00000591674.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.30G>A
  hgvsp: ENST00000590700.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.30G>A
  hgvsp: ENST00000591912.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.93G>A
  hgvsp: ENST00000587806.1:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.30G>A
  hgvsp: ENST00000252445.3:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.30G>A
  hgvsp: ENST00000586683.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.30G>A
  hgvsp: ENST00000589171.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8994
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro10Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

19-11665139-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665139
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665139
    reference: chr 19
allele count: 4
allele frequency: 3.298805832288711e-5
allele num: 121256
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.24A>G
  hgvsp: ENST00000590700.1:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.24A>G
  hgvsp: ENST00000586120.1:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.24A>G
  hgvsp: ENST00000586683.1:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.87A>G
  hgvsp: ENST00000587806.1:c.87A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.45A>G
  hgvsp: ENST00000591674.1:c.45A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.24A>G
  hgvsp: ENST00000589171.1:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.24A>G
  hgvsp: ENST00000252445.3:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.24A>G
  hgvsp: ENST00000591912.1:c.24A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2823
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg8Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

19-11665140-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665140
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665140
    reference: chr 19
allele count: 4
allele frequency: 3.298969072164949e-5
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.23G>A
  hgvsp: ENSP00000466665.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.23G>A
  hgvsp: ENSP00000467664.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.23G>A
  hgvsp: ENSP00000466732.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.23G>A
  hgvsp: ENSP00000252445.3:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.23G>A
  hgvsp: ENSP00000467914.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.86G>A
  hgvsp: ENSP00000465765.1:p.Arg29Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.23G>A
  hgvsp: ENSP00000467264.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.44G>A
  hgvsp: ENSP00000467330.1:p.Arg15Gln
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2821
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8995
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3674
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg8Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-11665155-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665155
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665155
    reference: chr 19
allele count: 2
allele frequency: 1.65264671371201e-5
allele num: 121018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.8G>A
  hgvsp: ENSP00000467914.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.8G>A
  hgvsp: ENSP00000467264.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.8G>A
  hgvsp: ENSP00000466732.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.71G>A
  hgvsp: ENSP00000465765.1:p.Arg24His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.29G>A
  hgvsp: ENSP00000467330.1:p.Arg10His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.8G>A
  hgvsp: ENSP00000466665.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.8G>A
  hgvsp: ENSP00000252445.3:p.Arg3His
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.8G>A
  hgvsp: ENSP00000467664.1:p.Arg3His
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8930
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg3His
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

19-11665156-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665156
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665156
    reference: chr 19
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.7C>T
  hgvsp: ENSP00000467664.1:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.70C>T
  hgvsp: ENSP00000465765.1:p.Arg24Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.7C>T
  hgvsp: ENSP00000467264.1:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.28C>T
  hgvsp: ENSP00000467330.1:p.Arg10Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.7C>T
  hgvsp: ENSP00000252445.3:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.7C>T
  hgvsp: ENSP00000466665.1:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.7C>T
  hgvsp: ENSP00000467914.1:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.7C>T
  hgvsp: ENSP00000466732.1:p.Arg3Cys
  variant of: http://identifiers.org/hgnc/28691
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32489
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg3Cys
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-11665163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 11665163
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 11665163
    reference: chr 19
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467664
  ensembl transcript: ENST00000586683
  gene symbol: ELOF1
  hgvsc: ENST00000586683.1:c.-1C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467264
  ensembl transcript: ENST00000590700
  gene symbol: ELOF1
  hgvsc: ENST00000590700.1:c.-1C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000465765
  ensembl transcript: ENST00000587806
  gene symbol: ELOF1
  hgvsc: ENST00000587806.1:c.63C>T
  hgvsp: ENST00000587806.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466665
  ensembl transcript: ENST00000591912
  gene symbol: ELOF1
  hgvsc: ENST00000591912.1:c.-1C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467914
  ensembl transcript: ENST00000586120
  gene symbol: ELOF1
  hgvsc: ENST00000586120.1:c.-1C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000467330
  ensembl transcript: ENST00000591674
  gene symbol: ELOF1
  hgvsc: ENST00000591674.1:c.21C>T
  hgvsp: ENST00000591674.1:c.21C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000466732
  ensembl transcript: ENST00000589171
  gene symbol: ELOF1
  hgvsc: ENST00000589171.1:c.-1C>T
  variant of: http://identifiers.org/hgnc/28691
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000130165
  ensembl protein: ENSP00000252445
  ensembl transcript: ENST00000252445
  gene symbol: ELOF1
  hgvsc: ENST00000252445.3:c.-1C>T
  variant of: http://identifiers.org/hgnc/28691
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp7Asp
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4782
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 257
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7779
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2647
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.503017021404341e-5
allele num: 66622
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: 16502
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.948e1

QD
type: SiteQuality
SIO_000300: 1.729e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

DP
type: SiteQuality
SIO_000300: 2.000824e6

VQSLOD
type: SiteQuality
SIO_000300: -1.006e-1

FS
type: SiteQuality
SIO_000300: 6.499e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.62e0

GenotypeQuality
all individuals: 2657
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15445
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3413
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4459
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15461
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 4804
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5815
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 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: 16502
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: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 8.753160863645205e-4
allele num: 10282
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.891e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.95e-1

QD
type: SiteQuality
SIO_000300: 1.375e1

FS
type: SiteQuality
SIO_000300: 1.41e0

VQSLOD
type: SiteQuality
SIO_000300: 2.1e0

DP
type: SiteQuality
SIO_000300: 2.004025e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
all individuals: 197
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4804
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15424
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2662
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5832
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15472
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7811
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4468
bin: 7.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 66672
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: 10294
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.059e0

QD
type: SiteQuality
SIO_000300: 3.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e0

DP
type: SiteQuality
SIO_000300: 2.004927e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.618000000000001e-1

FS
type: SiteQuality
SIO_000300: 3.322e0

MQ
type: SiteQuality
SIO_000300: 4.858e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

GenotypeQuality
all individuals: 99
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7808
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2662
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5835
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15475
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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

East Asian
type: Population
allele count: 4
allele frequency: 4.623208506703652e-4
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 2.491e0

MQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 2.005288e6

QD
type: SiteQuality
SIO_000300: 1.349e1

GenotypeQuality
all individuals: 3418
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15404
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5835
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4804
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2662
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
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: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e0

FS
type: SiteQuality
SIO_000300: 2.491e0

QD
type: SiteQuality
SIO_000300: 1.349e1

DP
type: SiteQuality
SIO_000300: 2.005288e6

GenotypeQuality
all individuals: 3418
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4474
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2661
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4807
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499100179964007e-5
allele num: 66680
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.006219e6

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.472e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.16e0

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.25e-1

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

GenotypeQuality
all individuals: 4478
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 87
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15488
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 5840
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15448
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4808
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2663
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7813
bin: 6.75e1
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: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999310158663508e-5
allele num: 66682
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: 8.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

QD
type: SiteQuality
SIO_000300: 1.348e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.33e0

FS
type: SiteQuality
SIO_000300: 5.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-2

DP
type: SiteQuality
SIO_000300: 2.006975e6

GenotypeQuality
all individuals: 91
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15382
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 1.15606936416185e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66692
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African
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Other
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MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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SIO_000300: 2.007957e6

ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

Latino
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South Asian
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Other
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East Asian
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European (Finnish)
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African
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FS
type: SiteQuality
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QD
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

Other
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 6
allele frequency: 8.995232526760817e-5
allele num: 66702
num of homozygotes: 0

East Asian
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ClippingRankSum
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SIO_000300: -3.4e-1

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

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

European (Non-Finnish)
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allele num: 66706
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African
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South Asian
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Other
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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MQ
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DP
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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African
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South Asian
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East Asian
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European (Finnish)
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Latino
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DP
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FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

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

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

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

South Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498800959232614e-5
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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Latino
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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VQSLOD
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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Latino
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allele frequency: 1.728011059270779e-4
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
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MQ
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VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11574
num of homozygotes: 0

East Asian
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African
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South Asian
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Other
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European (Non-Finnish)
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allele num: 66724
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European (Finnish)
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FS
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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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QD
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DP
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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MQ
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Latino
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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South Asian
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DP
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MQRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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MQ
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FS
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Other
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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DP
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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South Asian
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African
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East Asian
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European (Non-Finnish)
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Other
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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FS
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VQSLOD
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MQ
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DP
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Other
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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MQ
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FS
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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East Asian
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Other
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European (Finnish)
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South Asian
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African
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VQSLOD
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SIO_000300: 8.77e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.07e-1

QD
type: SiteQuality
SIO_000300: 1.152e1

FS
type: SiteQuality
SIO_000300: 1.173e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.409e0

DP
type: SiteQuality
SIO_000300: 2.017244e6

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7932
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5884
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3439
bin: 9.25e1
variant carriers: 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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 1.498576352465158e-5
allele num: 66730
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

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.59e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

FS
type: SiteQuality
SIO_000300: 2.684e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.01643e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 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: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.24e-1

FS
type: SiteQuality
SIO_000300: 1.163e0

VQSLOD
type: SiteQuality
SIO_000300: 2.77e0

QD
type: SiteQuality
SIO_000300: 1.357e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

DP
type: SiteQuality
SIO_000300: 2.017028e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.81e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

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

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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: 10402
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.178000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.331e1

DP
type: SiteQuality
SIO_000300: 2.016857e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15552
bin: 9.75e1
variant carriers: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
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: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

DP
type: SiteQuality
SIO_000300: 2.017213e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.821e0

FS
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 1.404e1

GenotypeQuality
all individuals: 15765
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
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: 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: 10402
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

QD
type: SiteQuality
SIO_000300: 1.295e1

FS
type: SiteQuality
SIO_000300: 8.455e0

DP
type: SiteQuality
SIO_000300: 2.017231e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.14e0

VQSLOD
type: SiteQuality
SIO_000300: -1.588e0

GenotypeQuality
all individuals: 5895
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4543
bin: 7.25e1
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: 0
allele frequency: 0.0e0
allele num: 10402
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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.017324e6

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-2

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.566e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15556
bin: 9.75e1
variant carriers: 3

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

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
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

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: 10402
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.703e0

FS
type: SiteQuality
SIO_000300: 9.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 2.017433e6

QD
type: SiteQuality
SIO_000300: 1.305e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.94e-1

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

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

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15557
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2683
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4867
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
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: 66738
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

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

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: -1.603e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.5e-3

QD
type: SiteQuality
SIO_000300: 1.719e1

DP
type: SiteQuality
SIO_000300: 2.017478e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.341e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 3438
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variant carriers: 0

GenotypeQuality
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variant carriers: 31

GenotypeQuality
all individuals: 4868
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 2684
bin: 8.75e1
variant carriers: 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

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: 32
allele frequency: 1.937984496124031e-3
allele num: 16512
num of homozygotes: 1

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.67e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

QD
type: SiteQuality
SIO_000300: 1.518e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.03e0

VQSLOD
type: SiteQuality
SIO_000300: 4.7e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

DP
type: SiteQuality
SIO_000300: 2.019298e6

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4872
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-2

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 3.587e0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.323e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.018963e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15584
bin: 9.75e1
variant carriers: 1

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: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
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

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: 66738
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.779e1

MQRankSum
type: SiteQuality
SIO_000300: -2.617e0

DP
type: SiteQuality
SIO_000300: 2.019129e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e-1

MQ
type: SiteQuality
SIO_000300: 5.614e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.54e-1

FS
type: SiteQuality
SIO_000300: 5.147e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.856e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
all individuals: 2686
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.429e1

VQSLOD
type: SiteQuality
SIO_000300: 8.93e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.17e-1

DP
type: SiteQuality
SIO_000300: 2.019581e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 1.459e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.851e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

GenotypeQuality
all individuals: 2946
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3807
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2473
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variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 65
allele frequency: 7.512713823393435e-3
allele num: 8652
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
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: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
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: 6612
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.193454e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.4e-1

QD
type: SiteQuality
SIO_000300: 1.36e1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.88e-1

MQ
type: SiteQuality
SIO_000300: 5.984e1

MQRankSum
type: SiteQuality
SIO_000300: 1.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.765e0

GenotypeQuality
all individuals: 1413
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 65
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 52
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GenotypeQuality
all individuals: 2946
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variant carriers: 0

GenotypeQuality
all individuals: 2469
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GenotypeQuality
all individuals: 990
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variant carriers: 0

GenotypeQuality
all individuals: 3802
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
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: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.18992e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.1186e1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

MQRankSum
type: SiteQuality
SIO_000300: -1.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.38e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 66
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 48
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 7631
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GenotypeQuality
all individuals: 3800
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GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
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: 10406
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.623e0

QD
type: SiteQuality
SIO_000300: 1.742e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.555e-1

FS
type: SiteQuality
SIO_000300: 6.984e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQRankSum
type: SiteQuality
SIO_000300: -3.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.18937e6

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 1408
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7628
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.143e0

DP
type: SiteQuality
SIO_000300: 2.188969e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.146e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

QD
type: SiteQuality
SIO_000300: 1.449e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.84e0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 56
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GenotypeQuality
all individuals: 60
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 40
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9185
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variant carriers: 0

South Asian
type: Population
allele count: 15
allele frequency: 9.090909090909091e-4
allele num: 16500
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: 12
allele frequency: 1.799208348326736e-4
allele num: 66696
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: 1.728309713100588e-4
allele num: 11572
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
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VQSLOD
type: SiteQuality
SIO_000300: 3.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

QD
type: SiteQuality
SIO_000300: 1.438e1

FS
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.96e-1

DP
type: SiteQuality
SIO_000300: 2.187877e6

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
all individuals: 7591
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variant carriers: 1

GenotypeQuality
all individuals: 56
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GenotypeQuality
all individuals: 9141
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GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 1396
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GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 31853
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variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 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

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: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.66e0

FS
type: SiteQuality
SIO_000300: 8.35e-1

QD
type: SiteQuality
SIO_000300: 1.463e1

ReadPosRankSum
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SIO_000300: -6.27e-1

MQ
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SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.184266e6

MQRankSum
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SIO_000300: -6.43e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
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DP
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: 1.17e0

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

South Asian
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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MQRankSum
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SIO_000300: 2.03e-1

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
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allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

MQRankSum
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DP
type: SiteQuality
SIO_000300: 2.181786e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
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SIO_000300: 4.96e-1

QD
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VQSLOD
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SIO_000300: -2.487e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.92e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 6.076072426783327e-5
allele num: 16458
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e-1

QD
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SIO_000300: 1.135e1

DP
type: SiteQuality
SIO_000300: 2.179525e6

ReadPosRankSum
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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: 10406
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
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MQRankSum
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BaseQRankSum
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FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 7
allele frequency: 4.255836575875486e-4
allele num: 16448
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
type: Population
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num of homozygotes: 0

DP
type: SiteQuality
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QD
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

East Asian
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allele frequency: 3.466605038132656e-4
allele num: 8654
num of homozygotes: 0

African
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VQSLOD
type: SiteQuality
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ClippingRankSum
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DP
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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QD
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SIO_000300: 1.103e1

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

Other
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num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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DP
type: SiteQuality
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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BaseQRankSum
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MQ
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ReadPosRankSum
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FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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

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

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

African
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FS
type: SiteQuality
SIO_000300: 1.5354e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 8.1e0

VQSLOD
type: SiteQuality
SIO_000300: -2.164e0

MQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.686e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.88e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 2.179349e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
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: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.057e1

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -3.894e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.599e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

DP
type: SiteQuality
SIO_000300: 2.179638e6

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
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: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

BaseQRankSum
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SIO_000300: 6.17e-1

MQ
type: SiteQuality
SIO_000300: 5.892e1

QD
type: SiteQuality
SIO_000300: 1.364e1

DP
type: SiteQuality
SIO_000300: 2.179807e6

MQRankSum
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SIO_000300: 9.3e-2

FS
type: SiteQuality
SIO_000300: 2.258e0

VQSLOD
type: SiteQuality
SIO_000300: 2.88e-1

GenotypeQuality
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variant carriers: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
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: 1.849e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.180301e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.061e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.01e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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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
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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: 8654
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

South Asian
type: Population
allele count: 1
allele frequency: 6.074596039363382e-5
allele num: 16462
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e-1

DP
type: SiteQuality
SIO_000300: 2.18024e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

MQRankSum
type: SiteQuality
SIO_000300: -4.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.787e0

QD
type: SiteQuality
SIO_000300: 9.67e0

VQSLOD
type: SiteQuality
SIO_000300: 5.09e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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
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num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.493555542233679e-5
allele num: 66724
num of homozygotes: 0

VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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FS
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DP
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-1

DP
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SIO_000300: 2.179487e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

QD
type: SiteQuality
SIO_000300: 1.387e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.908e0

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

Latino
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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: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.635e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 9.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

DP
type: SiteQuality
SIO_000300: 2.179366e6

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

Latino
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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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

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

East Asian
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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: 16442
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.179123e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.88e0

MQRankSum
type: SiteQuality
SIO_000300: -9.46e-1

FS
type: SiteQuality
SIO_000300: 4.504e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.332e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.56e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
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: 10406
num of homozygotes: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.282e0

VQSLOD
type: SiteQuality
SIO_000300: 2.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.012e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.179014e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

QD
type: SiteQuality
SIO_000300: 1.389e1

FS
type: SiteQuality
SIO_000300: 7.23e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66698
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.154e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

QD
type: SiteQuality
SIO_000300: 1.187e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.47e-1

DP
type: SiteQuality
SIO_000300: 2.179088e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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: 8654
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: 66698
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.825039542523421e-4
allele num: 16438
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

BaseQRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.154e0

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

DP
type: SiteQuality
SIO_000300: 2.179088e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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Other
type: Population
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

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

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

East Asian
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allele count: 4
allele frequency: 4.623208506703652e-4
allele num: 8652
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.69e-1

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 16410
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African
type: Population
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
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)
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allele count: 2
allele frequency: 2.999040307101727e-5
allele num: 66688
num of homozygotes: 0

FS
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -7.82e-1

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
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South Asian
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allele frequency: 1.231072263941894e-4
allele num: 16246
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Latino
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African
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Other
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European (Finnish)
type: Population
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allele frequency: 0.0e0
allele num: 6614
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66626
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BaseQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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DP
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FS
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MQRankSum
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ClippingRankSum
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VQSLOD
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 59
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7528
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3654
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8932
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
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: 902
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: 8650
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.156119182467373e-5
allele num: 16244
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.975e0

DP
type: SiteQuality
SIO_000300: 2.173009e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.552e0

QD
type: SiteQuality
SIO_000300: 1.22e1

VQSLOD
type: SiteQuality
SIO_000300: 5.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.89e-1