2-207988953-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988953
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988953
    reference: chr 2
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+115C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.278C>T
  hgvsp: ENSP00000309570.6:p.Ser93Leu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+115C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.278C>T
  hgvsp: ENSP00000397245.1:p.Ser93Leu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.278C>T
  hgvsp: ENSP00000398572.1:p.Ser93Leu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.194C>T
  hgvsp: ENSP00000413590.1:p.Ser65Leu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.194C>T
  hgvsp: ENSP00000403284.2:p.Ser65Leu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.179C>T
  hgvsp: ENSP00000387510.1:p.Ser60Leu
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8391
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10094
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8244
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser93Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

2-207988955-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988955
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988955
    reference: chr 2
allele count: 5
allele frequency: 4.129160128829796e-5
allele num: 121090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+113C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.276C>T
  hgvsp: ENST00000423015.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.276C>T
  hgvsp: ENST00000426163.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.276C>T
  hgvsp: ENST00000309446.6:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.192C>T
  hgvsp: ENST00000412414.2:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.177C>T
  hgvsp: ENST00000421199.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+113C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.192C>T
  hgvsp: ENST00000435602.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7906
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21845
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4191
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser92Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

2-207988973-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988973
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988973
    reference: chr 2
allele count: 5
allele frequency: 4.130251614928381e-5
allele num: 121058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.159G>A
  hgvsp: ENST00000421199.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.174G>A
  hgvsp: ENST00000435602.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.258G>A
  hgvsp: ENST00000426163.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.174G>A
  hgvsp: ENST00000412414.2:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.258G>A
  hgvsp: ENST00000423015.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+95G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.258G>A
  hgvsp: ENST00000309446.6:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+95G>A
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7935
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16957
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3846
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10099
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8337
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala86Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

2-207988979-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988979
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988979
    reference: chr 2
allele count: 1
allele frequency: 8.259138737012504e-6
allele num: 121078
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.252G>C
  hgvsp: ENST00000309446.6:c.252G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.252G>C
  hgvsp: ENST00000426163.1:c.252G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+89G>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.153G>C
  hgvsp: ENST00000421199.1:c.153G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.168G>C
  hgvsp: ENST00000412414.2:c.168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.168G>C
  hgvsp: ENST00000435602.1:c.168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+89G>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.252G>C
  hgvsp: ENST00000423015.1:c.252G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8387
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3851
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val84Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

2-207988981-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988981
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988981
    reference: chr 2
allele count: 3
allele frequency: 2.47794627812469e-5
allele num: 121068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.151G>A
  hgvsp: ENSP00000387510.1:p.Val51Met
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+87G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.250G>A
  hgvsp: ENSP00000309570.6:p.Val84Met
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+87G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.166G>A
  hgvsp: ENSP00000413590.1:p.Val56Met
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.250G>A
  hgvsp: ENSP00000397245.1:p.Val84Met
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.166G>A
  hgvsp: ENSP00000403284.2:p.Val56Met
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.250G>A
  hgvsp: ENSP00000398572.1:p.Val84Met
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7932
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10095
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val84Met
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

2-207988982-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988982
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988982
    reference: chr 2
allele count: 11
allele frequency: 9.089106292966684e-5
allele num: 121024
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.150C>T
  hgvsp: ENST00000421199.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.165C>T
  hgvsp: ENST00000412414.2:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.249C>T
  hgvsp: ENST00000309446.6:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+86C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.165C>T
  hgvsp: ENST00000435602.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.249C>T
  hgvsp: ENST00000426163.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.249C>T
  hgvsp: ENST00000423015.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+86C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13251
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7930
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8416
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro83Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

2-207988985-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988985
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988985
    reference: chr 2
allele count: 411
allele frequency: 3.394562093230698e-3
allele num: 121076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.246C>T
  hgvsp: ENST00000426163.1:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.147C>T
  hgvsp: ENST00000421199.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+83C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.162C>T
  hgvsp: ENST00000435602.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.162C>T
  hgvsp: ENST00000412414.2:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.246C>T
  hgvsp: ENST00000309446.6:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.246C>T
  hgvsp: ENST00000423015.1:c.246C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+83C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 5.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 13225
  bin: 3.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 4.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 7939
  bin: 3.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 17092
  bin: 2.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4827
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4161
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu82Leu
num of homozygotes: 2
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-207988988-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988988
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988988
    reference: chr 2
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.243G>T
  hgvsp: ENST00000309446.6:c.243G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.144G>T
  hgvsp: ENST00000421199.1:c.144G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.159G>T
  hgvsp: ENST00000435602.1:c.159G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.243G>T
  hgvsp: ENST00000426163.1:c.243G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.243G>T
  hgvsp: ENST00000423015.1:c.243G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+80G>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.159G>T
  hgvsp: ENST00000412414.2:c.159G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+80G>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17163
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu81Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/2-207988991-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988991
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988991
    reference: chr 2
allele count: 1
allele frequency: 8.259411599517651e-6
allele num: 121074
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+77G>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.156G>T
  hgvsp: ENST00000412414.2:c.156G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.240G>T
  hgvsp: ENST00000309446.6:c.240G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.156G>T
  hgvsp: ENST00000435602.1:c.156G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.141G>T
  hgvsp: ENST00000421199.1:c.141G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.240G>T
  hgvsp: ENST00000423015.1:c.240G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.240G>T
  hgvsp: ENST00000426163.1:c.240G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+77G>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3879
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4197
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22266
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu80Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

2-207988996-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988996
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988996
    reference: chr 2
allele count: 1
allele frequency: 8.260093834665961e-6
allele num: 121064
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.151C>G
  hgvsp: ENSP00000403284.2:p.Pro51Ala
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.136C>G
  hgvsp: ENSP00000387510.1:p.Pro46Ala
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.235C>G
  hgvsp: ENSP00000398572.1:p.Pro79Ala
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+72C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.235C>G
  hgvsp: ENSP00000309570.6:p.Pro79Ala
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.151C>G
  hgvsp: ENSP00000413590.1:p.Pro51Ala
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+72C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.235C>G
  hgvsp: ENSP00000397245.1:p.Pro79Ala
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2179
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro79Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

2-207988997-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988997
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988997
    reference: chr 2
allele count: 2
allele frequency: 1.652046059044126e-5
allele num: 121062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.150C>T
  hgvsp: ENST00000412414.2:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.234C>T
  hgvsp: ENST00000309446.6:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+71C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.150C>T
  hgvsp: ENST00000435602.1:c.150C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.234C>T
  hgvsp: ENST00000423015.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.135C>T
  hgvsp: ENST00000421199.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.234C>T
  hgvsp: ENST00000426163.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+71C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp78Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

2-207988997-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207988997
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207988997
    reference: chr 2
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.234C>A
  hgvsp: ENSP00000397245.1:p.Asp78Glu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+71C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.150C>A
  hgvsp: ENSP00000403284.2:p.Asp50Glu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.150C>A
  hgvsp: ENSP00000413590.1:p.Asp50Glu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.234C>A
  hgvsp: ENSP00000309570.6:p.Asp78Glu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+71C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.135C>A
  hgvsp: ENSP00000387510.1:p.Asp45Glu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.234C>A
  hgvsp: ENSP00000398572.1:p.Asp78Glu
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13333
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2183
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp78Glu
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

2-207989004-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989004
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989004
    reference: chr 2
allele count: 3
allele frequency: 2.479174930583102e-5
allele num: 121008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.143G>A
  hgvsp: ENSP00000413590.1:p.Arg48His
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+64G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.227G>A
  hgvsp: ENSP00000398572.1:p.Arg76His
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+64G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.227G>A
  hgvsp: ENSP00000397245.1:p.Arg76His
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.227G>A
  hgvsp: ENSP00000309570.6:p.Arg76His
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.143G>A
  hgvsp: ENSP00000403284.2:p.Arg48His
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.128G>A
  hgvsp: ENSP00000387510.1:p.Arg43His
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17363
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2622
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2181
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4842
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg76His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

2-207989005-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989005
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989005
    reference: chr 2
allele count: 15
allele frequency: 1.2393416617093e-4
allele num: 121032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+63C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.226C>T
  hgvsp: ENSP00000309570.6:p.Arg76Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.127C>T
  hgvsp: ENSP00000387510.1:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+63C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.142C>T
  hgvsp: ENSP00000403284.2:p.Arg48Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.226C>T
  hgvsp: ENSP00000398572.1:p.Arg76Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.226C>T
  hgvsp: ENSP00000397245.1:p.Arg76Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.142C>T
  hgvsp: ENSP00000413590.1:p.Arg48Cys
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17383
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13301
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7958
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22166
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2182
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10100
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2627
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg76Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

2-207989007-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989007
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989007
    reference: chr 2
allele count: 33
allele frequency: 2.726641768846878e-4
allele num: 121028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.224G>A
  hgvsp: ENSP00000397245.1:p.Arg75His
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+61G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.140G>A
  hgvsp: ENSP00000403284.2:p.Arg47His
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.224G>A
  hgvsp: ENSP00000398572.1:p.Arg75His
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.224G>A
  hgvsp: ENSP00000309570.6:p.Arg75His
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+61G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.140G>A
  hgvsp: ENSP00000413590.1:p.Arg47His
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.125G>A
  hgvsp: ENSP00000387510.1:p.Arg42His
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5124
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 17383
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13303
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8578
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8420
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg75His
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

2-207989008-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989008
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989008
    reference: chr 2
allele count: 3
allele frequency: 2.478929102627665e-5
allele num: 121020
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.223C>T
  hgvsp: ENSP00000309570.6:p.Arg75Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.223C>T
  hgvsp: ENSP00000397245.1:p.Arg75Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+60C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+60C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.223C>T
  hgvsp: ENSP00000398572.1:p.Arg75Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.139C>T
  hgvsp: ENSP00000403284.2:p.Arg47Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.139C>T
  hgvsp: ENSP00000413590.1:p.Arg47Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.124C>T
  hgvsp: ENSP00000387510.1:p.Arg42Cys
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13329
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8427
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg75Cys
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/2-207989011-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989011
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989011
    reference: chr 2
allele count: 1
allele frequency: 8.265145879824779e-6
allele num: 120990
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.136T>G
  hgvsp: ENSP00000413590.1:p.Phe46Val
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+57T>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.220T>G
  hgvsp: ENSP00000397245.1:p.Phe74Val
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.121T>G
  hgvsp: ENSP00000387510.1:p.Phe41Val
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.136T>G
  hgvsp: ENSP00000403284.2:p.Phe46Val
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.220T>G
  hgvsp: ENSP00000398572.1:p.Phe74Val
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+57T>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.220T>G
  hgvsp: ENSP00000309570.6:p.Phe74Val
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7940
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3913
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4892
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8470
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Phe74Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

2-207989023-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989023
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989023
    reference: chr 2
allele count: 1
allele frequency: 8.287063893262618e-6
allele num: 120670
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.124A>G
  hgvsp: ENSP00000403284.2:p.Ile42Val
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.208A>G
  hgvsp: ENSP00000309570.6:p.Ile70Val
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.208A>G
  hgvsp: ENSP00000397245.1:p.Ile70Val
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+45A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.124A>G
  hgvsp: ENSP00000413590.1:p.Ile42Val
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+45A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.109A>G
  hgvsp: ENSP00000387510.1:p.Ile37Val
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.208A>G
  hgvsp: ENSP00000398572.1:p.Ile70Val
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22197
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile70Val
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

2-207989027-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989027
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989027
    reference: chr 2
allele count: 3
allele frequency: 2.48954391555467e-5
allele num: 120504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.120G>A
  hgvsp: ENST00000412414.2:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+41G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.204G>A
  hgvsp: ENST00000309446.6:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.120G>A
  hgvsp: ENST00000435602.1:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+41G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.204G>A
  hgvsp: ENST00000423015.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.204G>A
  hgvsp: ENST00000426163.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.105G>A
  hgvsp: ENST00000421199.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7923
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13177
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4189
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10083
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro68Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

2-207989028-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989028
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989028
    reference: chr 2
allele count: 1
allele frequency: 8.299306178003518e-6
allele num: 120492
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+40C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.104C>G
  hgvsp: ENSP00000387510.1:p.Pro35Arg
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.203C>G
  hgvsp: ENSP00000309570.6:p.Pro68Arg
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.203C>G
  hgvsp: ENSP00000398572.1:p.Pro68Arg
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+40C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.203C>G
  hgvsp: ENSP00000397245.1:p.Pro68Arg
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.119C>G
  hgvsp: ENSP00000403284.2:p.Pro40Arg
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.119C>G
  hgvsp: ENSP00000413590.1:p.Pro40Arg
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13146
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8426
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro68Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-207989029-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989029
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989029
    reference: chr 2
allele count: 1
allele frequency: 8.301097405076952e-6
allele num: 120466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.202C>T
  hgvsp: ENSP00000397245.1:p.Pro68Ser
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.118C>T
  hgvsp: ENSP00000413590.1:p.Pro40Ser
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.118C>T
  hgvsp: ENSP00000403284.2:p.Pro40Ser
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.103C>T
  hgvsp: ENSP00000387510.1:p.Pro35Ser
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.202C>T
  hgvsp: ENSP00000398572.1:p.Pro68Ser
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.202C>T
  hgvsp: ENSP00000309570.6:p.Pro68Ser
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+39C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+39C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8459
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10079
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro68Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS

2-207989030-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989030
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989030
    reference: chr 2
allele count: 1
allele frequency: 8.308408109006315e-6
allele num: 120360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+38C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+38C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.102C>T
  hgvsp: ENST00000421199.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.201C>T
  hgvsp: ENST00000423015.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.117C>T
  hgvsp: ENST00000412414.2:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.201C>T
  hgvsp: ENST00000426163.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.201C>T
  hgvsp: ENST00000309446.6:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.117C>T
  hgvsp: ENST00000435602.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17293
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13096
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro67Pro
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

2-207989032-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989032
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989032
    reference: chr 2
allele count: 3
allele frequency: 2.497710432103905e-5
allele num: 120110
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.115C>G
  hgvsp: ENSP00000403284.2:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.199C>G
  hgvsp: ENSP00000398572.1:p.Pro67Ala
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.100C>G
  hgvsp: ENSP00000387510.1:p.Pro34Ala
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+36C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+36C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.115C>G
  hgvsp: ENSP00000413590.1:p.Pro39Ala
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.199C>G
  hgvsp: ENSP00000309570.6:p.Pro67Ala
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.199C>G
  hgvsp: ENSP00000397245.1:p.Pro67Ala
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13030
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17134
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4848
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21989
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro67Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

2-207989042-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989042
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989042
    reference: chr 2
allele count: 3
allele frequency: 2.514415984980555e-5
allele num: 119312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.90C>T
  hgvsp: ENST00000421199.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.189C>T
  hgvsp: ENST00000309446.6:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.105C>T
  hgvsp: ENST00000435602.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+26C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.189C>T
  hgvsp: ENST00000426163.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.105C>T
  hgvsp: ENST00000412414.2:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.189C>T
  hgvsp: ENST00000423015.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+26C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7846
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3886
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His63His
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-207989047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989047
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989047
    reference: chr 2
allele count: 1
allele frequency: 8.408307407718826e-6
allele num: 118930
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+21C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.184C>T
  hgvsp: ENSP00000398572.1:p.Leu62Phe
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+21C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.184C>T
  hgvsp: ENSP00000309570.6:p.Leu62Phe
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.100C>T
  hgvsp: ENSP00000403284.2:p.Leu34Phe
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.85C>T
  hgvsp: ENSP00000387510.1:p.Leu29Phe
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.100C>T
  hgvsp: ENSP00000413590.1:p.Leu34Phe
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.184C>T
  hgvsp: ENSP00000397245.1:p.Leu62Phe
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12467
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10080
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2261
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu62Phe
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum

2-207989048-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989048
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989048
    reference: chr 2
allele count: 11
allele frequency: 9.25847992593216e-5
allele num: 118810
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.183C>T
  hgvsp: ENST00000426163.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.99C>T
  hgvsp: ENST00000435602.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.183C>T
  hgvsp: ENST00000309446.6:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.183C>T
  hgvsp: ENST00000423015.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.99C>T
  hgvsp: ENST00000412414.2:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+20C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+20C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.84C>T
  hgvsp: ENST00000421199.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16353
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7832
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2630
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2194
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe61Phe
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: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

2-207989054-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989054
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989054
    reference: chr 2
allele count: 1
allele frequency: 8.458376330079678e-6
allele num: 118226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.93C>T
  hgvsp: ENST00000412414.2:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.177C>T
  hgvsp: ENST00000457962.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.93C>T
  hgvsp: ENST00000435602.1:c.93C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+14C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.177C>T
  hgvsp: ENST00000423015.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+14C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.177C>T
  hgvsp: ENST00000309446.6:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.78C>T
  hgvsp: ENST00000421199.1:c.78C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.177C>T
  hgvsp: ENST00000426163.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5090
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10080
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4153
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp59Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum

2-207989060-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989060
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989060
    reference: chr 2
allele count: 81
allele frequency: 6.884944920440637e-4
allele num: 117648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+8C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.171C>T
  hgvsp: ENST00000309446.6:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.87C>T
  hgvsp: ENST00000435602.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.171C>T
  hgvsp: ENST00000457962.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+8C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.72C>T
  hgvsp: ENST00000421199.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.87C>T
  hgvsp: ENST00000412414.2:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.171C>T
  hgvsp: ENST00000426163.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.171C>T
  hgvsp: ENST00000423015.1:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15769
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7811
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12292
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4148
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7953
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3246
  bin: 2.25e1
  variant carriers: 0
hgvs: c.163+8C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

2-207989067-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989067
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989067
    reference: chr 2
allele count: 1
allele frequency: 8.559005785887911e-6
allele num: 116836
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.164G>A
  hgvsp: ENSP00000309570.6:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.65G>A
  hgvsp: ENSP00000387510.1:p.Gly22Asp
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.164G>A
  hgvsp: ENSP00000397245.1:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.164G>A
  hgvsp: ENSP00000392015.1:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.80G>A
  hgvsp: ENSP00000403284.2:p.Gly27Asp
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.164G>A
  hgvsp: ENSP00000398572.1:p.Gly55Asp
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.80G>A
  hgvsp: ENSP00000413590.1:p.Gly27Asp
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.65+1G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.163+1G>A
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19974
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4743
  bin: 7.75e1
  variant carriers: 0
hgvs: c.163+1G>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-207989088-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989088
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989088
    reference: chr 2
allele count: 4
allele frequency: 3.5052666631614e-5
allele num: 114114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.143G>A
  hgvsp: ENSP00000392015.1:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.59G>A
  hgvsp: ENSP00000403284.2:p.Arg20Gln
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.44G>A
  hgvsp: ENSP00000387510.1:p.Arg15Gln
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.143G>A
  hgvsp: ENSP00000393268.1:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.143G>A
  hgvsp: ENSP00000309570.6:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.45G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.59G>A
  hgvsp: ENSP00000413590.1:p.Arg20Gln
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.143G>A
  hgvsp: ENSP00000397245.1:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.143G>A
  hgvsp: ENSP00000398572.1:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*206G>A
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7816
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg48Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-207989096-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989096
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989096
    reference: chr 2
allele count: 1
allele frequency: 8.839544586662894e-6
allele num: 113128
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*198G>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.37G>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.51G>C
  hgvsp: ENST00000435602.1:c.51G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.51G>C
  hgvsp: ENST00000412414.2:c.51G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.135G>C
  hgvsp: ENST00000426163.1:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.135G>C
  hgvsp: ENST00000458272.1:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.135G>C
  hgvsp: ENST00000457962.1:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.135G>C
  hgvsp: ENST00000423015.1:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.135G>C
  hgvsp: ENST00000309446.6:c.135G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.36G>C
  hgvsp: ENST00000421199.1:c.36G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12224
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr45Thr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

2-207989104-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989104
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989104
    reference: chr 2
allele count: 2
allele frequency: 1.785427342034316e-5
allele num: 112018
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.127C>T
  hgvsp: ENST00000309446.6:c.127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.127C>T
  hgvsp: ENST00000423015.1:c.127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.43C>T
  hgvsp: ENST00000412414.2:c.43C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.127C>T
  hgvsp: ENST00000458272.1:c.127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.43C>T
  hgvsp: ENST00000435602.1:c.43C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.127C>T
  hgvsp: ENST00000426163.1:c.127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.127C>T
  hgvsp: ENST00000457962.1:c.127C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.29C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.28C>T
  hgvsp: ENST00000421199.1:c.28C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*190C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu43Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

2-207989114-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989114
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989114
    reference: chr 2
allele count: 1
allele frequency: 9.004952723998199e-6
allele num: 111050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*180G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.117G>A
  hgvsp: ENST00000309446.6:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.117G>A
  hgvsp: ENST00000426163.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.117G>A
  hgvsp: ENST00000457962.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.33G>A
  hgvsp: ENST00000435602.1:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.33G>A
  hgvsp: ENST00000412414.2:c.33G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.117G>A
  hgvsp: ENST00000423015.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.117G>A
  hgvsp: ENST00000458272.1:c.117G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.18G>A
  hgvsp: ENST00000421199.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.19G>A
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu39Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

2-207989126-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989126
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989126
    reference: chr 2
allele count: 1
allele frequency: 9.048791081511509e-6
allele num: 110512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.6A>G
  hgvsp: ENST00000421199.1:c.6A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.105A>G
  hgvsp: ENST00000457962.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.105A>G
  hgvsp: ENST00000426163.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.21A>G
  hgvsp: ENST00000435602.1:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.105A>G
  hgvsp: ENST00000458272.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.105A>G
  hgvsp: ENST00000423015.1:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.21A>G
  hgvsp: ENST00000412414.2:c.21A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*168A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.7A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.105A>G
  hgvsp: ENST00000309446.6:c.105A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15056
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.105A>G
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

2-207989131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989131
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989131
    reference: chr 2
allele count: 17
allele frequency: 1.541530649256438e-4
allele num: 110280
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-3C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-3C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.19-3C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-3C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-3C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.19-3C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000118263
  ensembl transcript: ENST00000467833
  gene symbol: KLF7
  hgvsc: ENST00000467833.1:n.2C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-3C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-3C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-3C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3773
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12133
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14959
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2626
  bin: 9.25e1
  variant carriers: 0
hgvs: c.103-3C>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

2-207989138-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989138
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989138
    reference: chr 2
allele count: 3
allele frequency: 2.724845137967992e-5
allele num: 110098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-10C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-10C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-10C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-10C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-10C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-10C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.19-10C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-10C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.19-10C>G
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7799
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18500
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

2-207989144-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989144
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989144
    reference: chr 2
allele count: 1
allele frequency: 9.087439341342396e-6
allele num: 110042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-16C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-16C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-16C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-16C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-16C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-16C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.19-16C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.19-16C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-16C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14723
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3708
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18426
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

2-207989151-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989151
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989151
    reference: chr 2
allele count: 2
allele frequency: 1.819074818547287e-5
allele num: 109946
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.19-23C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-23C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-23C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-23C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-23C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-23C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-23C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.19-23C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-23C>G
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7796
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4668
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2623
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD

2-207989153-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989153
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989153
    reference: chr 2
allele count: 1
allele frequency: 9.098518761145685e-6
allele num: 109908
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-25C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-25C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-25C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.19-25C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-25C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.19-25C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-25C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-25C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-25C>A
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3836
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5080
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3861
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4659
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

2-207989159-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989159
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989159
    reference: chr 2
allele count: 1
allele frequency: 9.106307028247765e-6
allele num: 109814
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-31C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.19-31C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-31C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-31C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.19-31C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-31C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-31C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-31C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-31C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13864
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4011
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2190
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16440
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

2-207989167-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989167
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989166
    reference: chr 2
allele count: 1
allele frequency: 9.112945850875755e-6
allele num: 109734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-40delC
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-40delC
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-40delC
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-40delC
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-40delC
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-40delC
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.19-40delC
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.19-40delC
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-40delC
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 6530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15859
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2186
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: AG
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum

2-207989176-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989176
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989176
    reference: chr 2
allele count: 1
allele frequency: 9.126252578166353e-6
allele num: 109574
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-48T>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-48T>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-48T>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-48T>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.19-48T>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-48T>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-48T>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.19-48T>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-48T>A
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7731
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1679
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2766
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6938
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

2-207989179-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207989179
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207989179
    reference: chr 2
allele count: 1
allele frequency: 9.13191971216189e-6
allele num: 109506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-51G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-51G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.19-51G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.19-51G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-51G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-51G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-51G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-51G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-51G>A
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11986
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4584
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11272
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2585
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2623
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

2-207998775-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207998775
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207998775
    reference: chr 2
allele count: 2
allele frequency: 1.375515818431912e-4
allele num: 14540
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-9647C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-9647C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-9647C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.18+16C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-9647C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-9647C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-9647C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.18+16C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-9647C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

2-207998800-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207998800
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207998800
    reference: chr 2
allele count: 9993
allele frequency: 6.713920988981457e-1
allele num: 14884
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-9672G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-9672G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-9672G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-9672G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.9G>A
  hgvsp: ENST00000412414.2:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.9G>A
  hgvsp: ENST00000435602.1:c.9G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-9672G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-9672G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-9672G>A
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 354
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 2.5e0
  variant carriers: 664
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 6.75e1
  variant carriers: 527
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 5.75e1
  variant carriers: 429
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.75e1
  variant carriers: 557
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 8.75e1
  variant carriers: 461
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 487
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.5e0
  variant carriers: 545
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 9.75e1
  variant carriers: 1473
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.25e1
  variant carriers: 553
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.25e1
  variant carriers: 510
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 9.25e1
  variant carriers: 403
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 256
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 3.75e1
  variant carriers: 107
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 1.75e1
  variant carriers: 227
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 62
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 6.75e1
  variant carriers: 27
hgvs: p.Pro3Pro
num of homozygotes: 3356
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

2-207998803-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207998803
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207998803
    reference: chr 2
allele count: 3
allele frequency: 2.035002035002035e-4
allele num: 14742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-9675C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.6C>G
  hgvsp: ENSP00000403284.2:p.Phe2Leu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-9675C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-9675C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-9675C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-9675C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.6C>G
  hgvsp: ENSP00000413590.1:p.Phe2Leu
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-9675C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-9675C>G
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Phe2Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

2-207998809-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207998809
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207998809
    reference: chr 2
allele count: 0
allele frequency: 0.0e0
allele num: 14724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-9681C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-9681C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.-1C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-9681C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-9681C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-9681C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-9681C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-9681C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.-1C>A
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD

2-207998811-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207998811
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207998811
    reference: chr 2
allele count: 1
allele frequency: 6.788866259334691e-5
allele num: 14730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-9683G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-9683G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-9683G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-9683G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-9683G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.-3G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-9683G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-9683G>A
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3045
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-207998826-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207998826
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207998826
    reference: chr 2
allele count: 1
allele frequency: 6.78334011667345e-5
allele num: 14742
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.-18T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-9698T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-9698T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.-18T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-9698T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-9698T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-9698T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-9698T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-9698T>C
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2947
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

2-207998843-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 207998843
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 207998843
    reference: chr 2
allele count: 1
allele frequency: 6.789788158609451e-5
allele num: 14728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.103-9715G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000413590
  ensembl transcript: ENST00000435602
  gene symbol: KLF7
  hgvsc: ENST00000435602.1:c.-35G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000403284
  ensembl transcript: ENST00000412414
  gene symbol: KLF7
  hgvsc: ENST00000412414.2:c.-35G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.103-9715G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.103-9715G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.103-9715G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.4-9715G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.103-9715G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*166-9715G>A
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

2-208013859-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208013859
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208013859
    reference: chr 2
allele count: 1
allele frequency: 8.357011532675916e-5
allele num: 11966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.*12A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+16332A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+16332A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+16332A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+16332A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+18005A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+16332A>G
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4399
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP

2-208013872-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208013872
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208013872
    reference: chr 2
allele count: 3
allele frequency: 2.478110028085247e-4
allele num: 12106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.155G>A
  hgvsp: ENST00000451244.1:c.155G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+17992G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+16319G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+16319G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+16319G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+16319G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+16319G>A
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: stop retained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4674
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ter52Ter
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

2-208013892-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208013892
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208013892
    reference: chr 2
allele count: 2
allele frequency: 1.635858007524947e-4
allele num: 12226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+17972C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+16299C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+16299C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.135C>A
  hgvsp: ENSP00000412950.1:p.Asn45Lys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+16299C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+16299C>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+16299C>A
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn45Lys
num of homozygotes: 1
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS

2-208013901-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208013901
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208013901
    reference: chr 2
allele count: 10
allele frequency: 8.179290037624734e-4
allele num: 12226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+16290A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+17963A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+16290A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+16290A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.126A>G
  hgvsp: ENST00000451244.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+16290A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+16290A>G
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.25e1
  variant carriers: 1
hgvs: p.Gln42Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

2-208013904-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208013904
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208013904
    reference: chr 2
allele count: 1
allele frequency: 8.179290037624735e-5
allele num: 12226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+17960C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+16287C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+16287C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.123C>G
  hgvsp: ENST00000451244.1:c.123C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+16287C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+16287C>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+16287C>G
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu41Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

2-208013918-TAATTTTCTGAGGAGAAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208013918
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208013900
    reference: chr 2
allele count: 1
allele frequency: 8.198065256599443e-5
allele num: 12198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: coding_sequence_variant
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  variant of: http://identifiers.org/hgnc/6350
canonical: false
consequence: splice acceptor
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1242
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.25e1
  variant carriers: 0
hgvs: c.103-12_108delTTTTCTCCTCAGAAAATT
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: TAATTTTCTGAGGAGAAAA
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

2-208013932-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208013932
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208013933
    reference: chr 2
allele count: 3
allele frequency: 2.477700693756194e-4
allele num: 12108
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.103-9dupT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+17931dupT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+16258dupT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+16258dupT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+16258dupT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+16258dupT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+16258dupT
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

2-208013949-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208013949
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208013949
    reference: chr 2
allele count: 1
allele frequency: 8.471704506946798e-5
allele num: 11804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+17915C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+16242C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+16242C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.103-25C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+16242C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+16242C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+16242C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

2-208013974-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208013974
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208013974
    reference: chr 2
allele count: 1
allele frequency: 9.082652134423252e-5
allele num: 11010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+16217C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.103-50C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+16217C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+17890C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+16217C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+16217C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+16217C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 929
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1650
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

2-208030140-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030140
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030140
    reference: chr 2
allele count: 2
allele frequency: 1.666694444907415e-5
allele num: 119998
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.102+51A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+51A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+51A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+51A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+51A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1724A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+51A>G
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14044
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14598
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4309
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13147
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1333
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

2-208030141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030141
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030141
    reference: chr 2
allele count: 1
allele frequency: 8.327226700419692e-6
allele num: 120088
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+50C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+50C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+50C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+50C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+50C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1723C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.102+50C>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2186
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15066
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/2-208030142-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030142
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030142
    reference: chr 2
allele count: 1
allele frequency: 8.333055564814507e-6
allele num: 120004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+49G>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+49G>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+49G>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+49G>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+49G>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.102+49G>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1722G>T
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2231
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3058
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3128
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

2-208030152-GCCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030152
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030149
    reference: chr 2
allele count: 1
allele frequency: 8.322929671244279e-6
allele num: 120150
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+36_102+38delTGG
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+36_102+38delTGG
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+36_102+38delTGG
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+36_102+38delTGG
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1709_3+1711delTGG
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+36_102+38delTGG
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.102+36_102+38delTGG
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1217
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2954
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: GCCA
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/2-208030155-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030155
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030155
    reference: chr 2
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+36T>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1709T>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+36T>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+36T>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+36T>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+36T>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.102+36T>G
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3096
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2104
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13122
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7462
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4067
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

2-208030159-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030159
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030159
    reference: chr 2
allele count: 2
allele frequency: 1.660274609420398e-5
allele num: 120462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+32G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+32G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+32G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+32G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1705G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+32G>A
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.102+32G>A
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13125
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2967
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

2-208030170-CAAGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030170
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030166
    reference: chr 2
allele count: 1
allele frequency: 8.279379377721846e-6
allele num: 120782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+17_102+20delACTT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+17_102+20delACTT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+17_102+20delACTT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1690_3+1693delACTT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+17_102+20delACTT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.102+17_102+20delACTT
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+17_102+20delACTT
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4099
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: CAAGT
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

2-208030174-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030174
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030174
    reference: chr 2
allele count: 1
allele frequency: 8.273762245168123e-6
allele num: 120864
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+17A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1690A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+17A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+17A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+17A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+17A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.102+17A>G
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4097
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

2-208030182-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030182
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030182
    reference: chr 2
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.102+9T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1682T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.102+9T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.102+9T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.102+9T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.102+9T>C
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.102+9T>C
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16197
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4093
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3166
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25380
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

2-208030211-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030211
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030211
    reference: chr 2
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.82C>T
  hgvsp: ENST00000458272.1:c.82C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.82C>T
  hgvsp: ENST00000457962.1:c.82C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1653C>T
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.82C>T
  hgvsp: ENST00000426163.1:c.82C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.82C>T
  hgvsp: ENST00000451244.1:c.82C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.82C>T
  hgvsp: ENST00000309446.6:c.82C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.82C>T
  hgvsp: ENST00000423015.1:c.82C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3194
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4110
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25836
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu28Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

2-208030221-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030221
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030221
    reference: chr 2
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.72T>C
  hgvsp: ENST00000423015.1:c.72T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.72T>C
  hgvsp: ENST00000426163.1:c.72T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.72T>C
  hgvsp: ENST00000457962.1:c.72T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.72T>C
  hgvsp: ENST00000309446.6:c.72T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.72T>C
  hgvsp: ENST00000451244.1:c.72T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.72T>C
  hgvsp: ENST00000458272.1:c.72T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1643T>C
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1491
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7732
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala24Ala
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-208030231-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 208030231
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 208030231
    reference: chr 2
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000412950
  ensembl transcript: ENST00000451244
  gene symbol: KLF7
  hgvsc: ENST00000451244.1:c.62A>G
  hgvsp: ENSP00000412950.1:p.Tyr21Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000387510
  ensembl transcript: ENST00000421199
  gene symbol: KLF7
  hgvsc: ENST00000421199.1:c.3+1633A>G
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000393268
  ensembl transcript: ENST00000458272
  gene symbol: KLF7
  hgvsc: ENST00000458272.1:c.62A>G
  hgvsp: ENSP00000393268.1:p.Tyr21Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000392015
  ensembl transcript: ENST00000457962
  gene symbol: KLF7
  hgvsc: ENST00000457962.1:c.62A>G
  hgvsp: ENSP00000392015.1:p.Tyr21Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000397245
  ensembl transcript: ENST00000426163
  gene symbol: KLF7
  hgvsc: ENST00000426163.1:c.62A>G
  hgvsp: ENSP00000397245.1:p.Tyr21Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000398572
  ensembl transcript: ENST00000423015
  gene symbol: KLF7
  hgvsc: ENST00000423015.1:c.62A>G
  hgvsp: ENSP00000398572.1:p.Tyr21Cys
  variant of: http://identifiers.org/hgnc/6350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000118263
  ensembl protein: ENSP00000309570
  ensembl transcript: ENST00000309446
  gene symbol: KLF7
  hgvsc: ENST00000309446.6:c.62A>G
  hgvsp: ENSP00000309570.6:p.Tyr21Cys
  variant of: http://identifiers.org/hgnc/6350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr21Cys
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 443
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3813
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21612
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4809
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.023e0

QD
type: SiteQuality
SIO_000300: 1.002e1

VQSLOD
type: SiteQuality
SIO_000300: -9.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.980206e6

FS
type: SiteQuality
SIO_000300: 9.901e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 421
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3819
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 528
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4814
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 183
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10092
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 8277
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.789717461787865e-4
allele num: 8636
num of homozygotes: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.784e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-1

FS
type: SiteQuality
SIO_000300: 2.214e0

DP
type: SiteQuality
SIO_000300: 1.97971e6

MQRankSum
type: SiteQuality
SIO_000300: 1.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.275e1

GenotypeQuality
all individuals: 21597
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 243
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4165
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4831
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2577
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.63284688441047e-4
allele num: 8634
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.05e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-1

DP
type: SiteQuality
SIO_000300: 1.981315e6

QD
type: SiteQuality
SIO_000300: 2.968e1

GenotypeQuality
all individuals: 495
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2167
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4840
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2581
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10096
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21890
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.417e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

FS
type: SiteQuality
SIO_000300: 8.579000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 7.0e-3

QD
type: SiteQuality
SIO_000300: 1.237e1

DP
type: SiteQuality
SIO_000300: 1.982906e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.1e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.87e-1

GenotypeQuality
all individuals: 4835
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8378
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21824
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2586
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4162
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 239
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3850
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.473026163463765e-4
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.27e-1

FS
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.566e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

DP
type: SiteQuality
SIO_000300: 1.98379e6

QD
type: SiteQuality
SIO_000300: 1.196e1

GenotypeQuality
all individuals: 2166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22093
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2587
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10096
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 4833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.651403693139168e-4
allele num: 66610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 6.999e0

DP
type: SiteQuality
SIO_000300: 1.984623e6

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

VQSLOD
type: SiteQuality
SIO_000300: -1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 2.727e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 458
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8412
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10397
bin: 9.75e1
variant carriers: 407

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3844
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 306
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21969
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 3.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 15
allele frequency: 1.298926220990648e-3
allele num: 11548
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 7.795751315533034e-4
allele num: 10262
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.030670384289005e-4
allele num: 16498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 108
allele frequency: 1.643335362142422e-2
allele num: 6572
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 269
allele frequency: 4.035887895336974e-3
allele num: 66652
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.63716814159292e-3
allele num: 904
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.153e0

DP
type: SiteQuality
SIO_000300: 1.987917e6

QD
type: SiteQuality
SIO_000300: 1.284e1

VQSLOD
type: SiteQuality
SIO_000300: 5.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.56e-1

GenotypeQuality
all individuals: 10081
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8454
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3876
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4188
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4869
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22149
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2609
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.518e0

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.100000000000001e-1

FS
type: SiteQuality
SIO_000300: 2.884e0

QD
type: SiteQuality
SIO_000300: 1.22e1

DP
type: SiteQuality
SIO_000300: 1.985551e6

GenotypeQuality
all individuals: 254
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2613
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4857
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10086
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8487
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 2.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.74089226573154e-5
allele num: 10266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.487e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.281e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 4.288e0

QD
type: SiteQuality
SIO_000300: 1.203e1

DP
type: SiteQuality
SIO_000300: 1.986346e6

VQSLOD
type: SiteQuality
SIO_000300: -1.363e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

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

GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2619
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4863
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22061
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3873
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4206
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8452
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.908e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e-1

FS
type: SiteQuality
SIO_000300: 2.277e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

DP
type: SiteQuality
SIO_000300: 1.986986e6

QD
type: SiteQuality
SIO_000300: 1.357e1

GenotypeQuality
all individuals: 22065
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4206
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2183
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8465
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10088
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4866
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3877
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2621
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001200480192077e-5
allele num: 66640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.69e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.98717e6

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.225e0

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

GenotypeQuality
all individuals: 439
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4866
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22065
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10088
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4206
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8465
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

QD
type: SiteQuality
SIO_000300: 1.314e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.98717e6

MQRankSum
type: SiteQuality
SIO_000300: -6.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.225e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

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

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 307
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10091
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 193
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8408
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4209
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21966
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3878
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31535077564251e-4
allele num: 8638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

QD
type: SiteQuality
SIO_000300: 8.84e0

FS
type: SiteQuality
SIO_000300: 4.603e0

MQRankSum
type: SiteQuality
SIO_000300: -2.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.988163e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

GenotypeQuality
all individuals: 268
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4863
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8453
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 286
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3895
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

African
type: Population
allele count: 15
allele frequency: 1.460564751703992e-3
allele num: 10270
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

FS
type: SiteQuality
SIO_000300: 2.481e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 1.988419e6

QD
type: SiteQuality
SIO_000300: 1.358e1

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4216
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10117
bin: 9.75e1
variant carriers: 33

GenotypeQuality
all individuals: 4856
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2625
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22087
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 275
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3896
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 30
allele frequency: 1.821272462360369e-3
allele num: 16472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.18e1

DP
type: SiteQuality
SIO_000300: 1.988526e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2182
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 212
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10087
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 22347
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4219
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3900
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variant carriers: 0

GenotypeQuality
all individuals: 4866
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2623
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10268
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.821714840903571e-4
allele num: 16468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.898e0

QD
type: SiteQuality
SIO_000300: 1.357e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.03e-2

MQ
type: SiteQuality
SIO_000300: 5.945e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

DP
type: SiteQuality
SIO_000300: 1.989051e6

MQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

GenotypeQuality
all individuals: 237
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2190
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2626
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4237
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22449
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10084
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 222
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.6e-1

QD
type: SiteQuality
SIO_000300: 1.093e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

FS
type: SiteQuality
SIO_000300: 7.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.988817e6

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 690
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 194
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10081
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4225
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3907
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2632
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8458
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.773260359655981e-5
allele num: 10232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66514
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 1.984953e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.25e-1

FS
type: SiteQuality
SIO_000300: 2.88e0

QD
type: SiteQuality
SIO_000300: 1.635e1

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 787
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22129
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2184
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variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504392827055001e-5
allele num: 66472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.240079365079365e-4
allele num: 16128
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.609e0

FS
type: SiteQuality
SIO_000300: 1.2482e1

MQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

QD
type: SiteQuality
SIO_000300: 1.159e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.13e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

DP
type: SiteQuality
SIO_000300: 1.983467e6

GenotypeQuality
all individuals: 194
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4191
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3885
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10077
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504845602841149e-5
allele num: 66452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.187e1

MQ
type: SiteQuality
SIO_000300: 5.89e1

DP
type: SiteQuality
SIO_000300: 1.982939e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.444e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

GenotypeQuality
all individuals: 156
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 213
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 4858
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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
all individuals: 2191
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.778994719342852e-5
allele num: 10226
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16096
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66458
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.48e-1

DP
type: SiteQuality
SIO_000300: 1.981852e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.39e-1

QD
type: SiteQuality
SIO_000300: 1.337e1

VQSLOD
type: SiteQuality
SIO_000300: 6.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 2.985e0

GenotypeQuality
all individuals: 2193
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4850
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 4204
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GenotypeQuality
all individuals: 10078
bin: 9.75e1
variant carriers: 1

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16012
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505253334136135e-5
allele num: 66434
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.598e1

DP
type: SiteQuality
SIO_000300: 1.978922e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.658e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 1.4769e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.836e0

GenotypeQuality
all individuals: 2190
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 2629
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 213
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GenotypeQuality
all individuals: 8355
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 3896
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variant carriers: 0

GenotypeQuality
all individuals: 10076
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variant carriers: 3

GenotypeQuality
all individuals: 139
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variant carriers: 0

GenotypeQuality
all individuals: 187
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variant carriers: 0

GenotypeQuality
all individuals: 4195
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.893939393939394e-4
allele num: 15840
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

QD
type: SiteQuality
SIO_000300: 1.484e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.55e-1

FS
type: SiteQuality
SIO_000300: 7.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.57e-1

DP
type: SiteQuality
SIO_000300: 1.973968e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511121856866538e-5
allele num: 66176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.311131506490101e-4
allele num: 15254
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 7.15e-1

DP
type: SiteQuality
SIO_000300: 1.957073e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.99e-1

QD
type: SiteQuality
SIO_000300: 9.9e0

FS
type: SiteQuality
SIO_000300: 2.202e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.56e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 129
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4165
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.67913438418381e-5
allele num: 14972
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66092
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.03e-1

DP
type: SiteQuality
SIO_000300: 1.94916e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.561e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.03e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 261
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.25e1
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GenotypeQuality
all individuals: 4795
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GenotypeQuality
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 8086
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10089
bin: 9.75e1
variant carriers: 11

GenotypeQuality
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GenotypeQuality
all individuals: 100
bin: 4.25e1
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GenotypeQuality
all individuals: 3886
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 11
allele frequency: 7.387508394895903e-4
allele num: 14890
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66066
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.22e-1

QD
type: SiteQuality
SIO_000300: 1.448e1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

DP
type: SiteQuality
SIO_000300: 1.94713e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 1.782e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2193
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 2.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.163e0

MQRankSum
type: SiteQuality
SIO_000300: 7.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

QD
type: SiteQuality
SIO_000300: 2.315e1

DP
type: SiteQuality
SIO_000300: 1.937402e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 80

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4746
bin: 7.75e1
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GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 4.331254331254331e-4
allele num: 11544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
type: Population
allele count: 76
allele frequency: 7.49063670411985e-3
allele num: 10146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14086
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65772
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.171e0

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.88e0

DP
type: SiteQuality
SIO_000300: 1.930552e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.32e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.272e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

GenotypeQuality
all individuals: 4129
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 10083
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524669146795145e-5
allele num: 65588
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13506
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

QD
type: SiteQuality
SIO_000300: 1.176e1

DP
type: SiteQuality
SIO_000300: 1.919971e6

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.72e-1

FS
type: SiteQuality
SIO_000300: 8.057e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.176e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-1

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2200
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 115
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GenotypeQuality
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GenotypeQuality
all individuals: 978
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.160670280926565e-5
allele num: 64928
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.464e0

DP
type: SiteQuality
SIO_000300: 1.898937e6

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

QD
type: SiteQuality
SIO_000300: 1.351e1

FS
type: SiteQuality
SIO_000300: 1.1721e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

GenotypeQuality
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bin: 9.75e1
variant carriers: 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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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.546981838433217e-5
allele num: 64642
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.891868e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

VQSLOD
type: SiteQuality
SIO_000300: -2.055e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.64e-1

FS
type: SiteQuality
SIO_000300: 1.0009e1

MQRankSum
type: SiteQuality
SIO_000300: -1.24e0

QD
type: SiteQuality
SIO_000300: 5.08e0

MQ
type: SiteQuality
SIO_000300: 5.877e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.89e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 2
allele frequency: 2.340823970037453e-4
allele num: 8544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9948
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.101e0

FS
type: SiteQuality
SIO_000300: 6.075e0

VQSLOD
type: SiteQuality
SIO_000300: 8.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

DP
type: SiteQuality
SIO_000300: 1.884098e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

QD
type: SiteQuality
SIO_000300: 9.31e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 2193
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559235350983878e-5
allele num: 64134
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.149e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

DP
type: SiteQuality
SIO_000300: 1.874908e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.351e0

FS
type: SiteQuality
SIO_000300: 4.057e0

VQSLOD
type: SiteQuality
SIO_000300: 5.74e-1

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2626
bin: 9.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.173984503404555e-4
allele num: 8518
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9846
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9282
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63996
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.86682e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.41e-1

FS
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VQSLOD
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InbreedingCoeff
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SIO_000300: -2.7e-3

MQRankSum
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SIO_000300: -3.21e-1

QD
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SIO_000300: 1.305e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
allele num: 8510
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Other
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.018744906275469e-4
allele num: 9816
num of homozygotes: 0

South Asian
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allele count: 13
allele frequency: 1.418594500218245e-3
allele num: 9164
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11466
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.692779376798899e-5
allele num: 63928
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.47e-1

MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: 3.4e-1

QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-1

DP
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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variant carriers: 3

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63870
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.06435137895812e-4
allele num: 9790
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South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
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MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

FS
type: SiteQuality
SIO_000300: 2.079e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

QD
type: SiteQuality
SIO_000300: 1.264e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.73e-1

DP
type: SiteQuality
SIO_000300: 1.856493e6

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.566219771958401e-5
allele num: 63848
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9784
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.02e-1

FS
type: SiteQuality
SIO_000300: 7.079e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e0

MQRankSum
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

QD
type: SiteQuality
SIO_000300: 1.122e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.852537e6

VQSLOD
type: SiteQuality
SIO_000300: -4.715e-1

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.134206732276061e-5
allele num: 63812
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9024
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

FS
type: SiteQuality
SIO_000300: 2.208e0

DP
type: SiteQuality
SIO_000300: 1.845533e6

MQRankSum
type: SiteQuality
SIO_000300: 4.44e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.547e1

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: 8.75e1
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

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

African
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allele frequency: 1.025430680885972e-4
allele num: 9752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63792
num of homozygotes: 0

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

Latino
type: Population
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
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FS
type: SiteQuality
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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VQSLOD
type: SiteQuality
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ClippingRankSum
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MQ
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 1.028383381324558e-4
allele num: 9724
num of homozygotes: 0

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

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

East Asian
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6604
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South Asian
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allele count: 0
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
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FS
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -1.15e-1

MQRankSum
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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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GenotypeQuality
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Other
type: Population
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num of homozygotes: 0

East Asian
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allele frequency: 1.178411501296253e-4
allele num: 8486
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South Asian
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European (Non-Finnish)
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allele count: 0
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European (Finnish)
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Latino
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African
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VQSLOD
type: SiteQuality
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
type: SiteQuality
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QD
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FS
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BaseQRankSum
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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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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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
type: Population
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Other
type: Population
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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
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South Asian
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BaseQRankSum
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SIO_000300: 2.17e0

ClippingRankSum
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VQSLOD
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FS
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DP
type: SiteQuality
SIO_000300: 1.808431e6

QD
type: SiteQuality
SIO_000300: 1.249e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.24e-1

GenotypeQuality
all individuals: 1441
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10077
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 527
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3887
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6768
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2059
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3832
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.572228161750833e-5
allele num: 63604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8972
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.602e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.117e0

MQRankSum
type: SiteQuality
SIO_000300: -3.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.375e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e0

DP
type: SiteQuality
SIO_000300: 1.807844e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.029e0

QD
type: SiteQuality
SIO_000300: 1.471e1

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2697
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3001
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.626050420168067e-4
allele num: 7616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.01e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.972e0

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

FS
type: SiteQuality
SIO_000300: 5.744e0

MQ
type: SiteQuality
SIO_000300: 5.812e1

VQSLOD
type: SiteQuality
SIO_000300: -1.409e0

QD
type: SiteQuality
SIO_000300: 9.98e0

DP
type: SiteQuality
SIO_000300: 3.43921e5

GenotypeQuality
all individuals: 1082
bin: 7.5e0
variant carriers: 381

GenotypeQuality
all individuals: 165
bin: 2.25e1
variant carriers: 122

GenotypeQuality
all individuals: 104
bin: 8.25e1
variant carriers: 21

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 30

GenotypeQuality
all individuals: 6694
bin: 9.75e1
variant carriers: 6427

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 21

GenotypeQuality
all individuals: 494
bin: 2.5e0
variant carriers: 11

GenotypeQuality
all individuals: 126
bin: 6.25e1
variant carriers: 22

GenotypeQuality
all individuals: 247
bin: 1.25e1
variant carriers: 235

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 66

GenotypeQuality
all individuals: 107
bin: 7.75e1
variant carriers: 21

GenotypeQuality
all individuals: 58
bin: 7.25e1
variant carriers: 10

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 38

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 29

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

Latino
type: Population
allele count: 145
allele frequency: 7.25e-1
allele num: 200
num of homozygotes: 56

European (Finnish)
type: Population
allele count: 1134
allele frequency: 7.141057934508817e-1
allele num: 1588
num of homozygotes: 400

African
type: Population
allele count: 390
allele frequency: 6.170886075949367e-1
allele num: 632
num of homozygotes: 117

Other
type: Population
allele count: 131
allele frequency: 6.55e-1
allele num: 200
num of homozygotes: 46

South Asian
type: Population
allele count: 5217
allele frequency: 6.844660194174758e-1
allele num: 7622
num of homozygotes: 1797

European (Non-Finnish)
type: Population
allele count: 2808
allele frequency: 6.413887619917771e-1
allele num: 4378
num of homozygotes: 887

East Asian
type: Population
allele count: 168
allele frequency: 6.363636363636364e-1
allele num: 264
num of homozygotes: 53

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.532e-1

FS
type: SiteQuality
SIO_000300: 5.23e-1

DP
type: SiteQuality
SIO_000300: 5.60293e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

QD
type: SiteQuality
SIO_000300: 2.08e1

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

MQ
type: SiteQuality
SIO_000300: 5.637e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.32e-1

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2811
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1922
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1390
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 1.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.937007874015748e-4
allele num: 7620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4278
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.55e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.72e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.429e-1

DP
type: SiteQuality
SIO_000300: 3.6361e5

QD
type: SiteQuality
SIO_000300: 8.76e0

GenotypeQuality
all individuals: 129
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 657
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 435
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3033
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1104
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 9.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.85e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.337e1

DP
type: SiteQuality
SIO_000300: 3.63837e5

MQ
type: SiteQuality
SIO_000300: 3.7e1

VQSLOD
type: SiteQuality
SIO_000300: -2.589e0

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

GenotypeQuality
all individuals: 120
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1105
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312335958005249e-4
allele num: 7620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.896e1

DP
type: SiteQuality
SIO_000300: 3.63856e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.14e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.446e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e0

QD
type: SiteQuality
SIO_000300: 1.015e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1397
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1917
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 1
allele frequency: 4.0e-3
allele num: 250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4272
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.16e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.25e0

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

MQ
type: SiteQuality
SIO_000300: 5.628e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.22e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.439e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.32e-1

DP
type: SiteQuality
SIO_000300: 3.634e5

GenotypeQuality
all individuals: 2628
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1364
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1083
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1897
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 273
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4264
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1586
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: -1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.036e0

FS
type: SiteQuality
SIO_000300: 3.634e0

MQRankSum
type: SiteQuality
SIO_000300: -2.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

DP
type: SiteQuality
SIO_000300: 3.61359e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.15e-2

QD
type: SiteQuality
SIO_000300: 1.037e1

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

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1436
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.862049227246708e-4
allele num: 3494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.794e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

QD
type: SiteQuality
SIO_000300: 1.263e1

MQ
type: SiteQuality
SIO_000300: 5.911e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.31e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.39e-1

DP
type: SiteQuality
SIO_000300: 1.5695e5

GenotypeQuality
all individuals: 175
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 129
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1381
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 128
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.995737879595098e-4
allele num: 7508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.951e1

MQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

DP
type: SiteQuality
SIO_000300: 1.60389e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.058e0

FS
type: SiteQuality
SIO_000300: 6.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

QD
type: SiteQuality
SIO_000300: 1.272e1

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

GenotypeQuality
all individuals: 80
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 127
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4814
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 521
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3554
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 2.633658151171978e-4
allele num: 7594
num of homozygotes: 1

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

DP
type: SiteQuality
SIO_000300: 1.61937e5

QD
type: SiteQuality
SIO_000300: 2.648e1

MQ
type: SiteQuality
SIO_000300: 5.855e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.66e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.129e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

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

GenotypeQuality
all individuals: 4803
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 128
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 9.75e1
variant carriers: 10

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.612903225806452e-2
allele num: 558
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.317523056653491e-4
allele num: 7590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.13e0

FS
type: SiteQuality
SIO_000300: 5.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.27e0

DP
type: SiteQuality
SIO_000300: 1.619e5

QD
type: SiteQuality
SIO_000300: 1.363e1

GenotypeQuality
all individuals: 69
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1322
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 127
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4809
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3556
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.792114695340502e-3
allele num: 558
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7590
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.11e-2

QD
type: SiteQuality
SIO_000300: 1.366e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.21e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.61733e5

GenotypeQuality
all individuals: 69
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 194
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4746
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.319609395618897e-4
allele num: 7578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3542
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.72e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

QD
type: SiteQuality
SIO_000300: 7.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.195e0

MQ
type: SiteQuality
SIO_000300: 5.508e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.438e0

VQSLOD
type: SiteQuality
SIO_000300: -1.297e0

DP
type: SiteQuality
SIO_000300: 1.612e5

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

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 68
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4548
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 3.994673768308921e-4
allele num: 7510
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.9e-1

DP
type: SiteQuality
SIO_000300: 1.59238e5

FS
type: SiteQuality
SIO_000300: 4.641e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.99e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

QD
type: SiteQuality
SIO_000300: 1.045e1

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

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 1.368738023542294e-4
allele num: 7306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.046e0

DP
type: SiteQuality
SIO_000300: 1.41631e5

VQSLOD
type: SiteQuality
SIO_000300: -9.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.35e-2

QD
type: SiteQuality
SIO_000300: 1.568e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.544e0

GenotypeQuality
all individuals: 222
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6724
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.376344086021506e-3
allele num: 186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.46e-2

DP
type: SiteQuality
SIO_000300: 1.2096e5

VQSLOD
type: SiteQuality
SIO_000300: -1.716e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.684e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.22e-1

QD
type: SiteQuality
SIO_000300: 9.31e0

MQ
type: SiteQuality
SIO_000300: 5.79e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.25e-1

GenotypeQuality
all individuals: 3136
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
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GenotypeQuality
all individuals: 7132
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2591
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3165
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1078
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.030945958233565e-5
allele num: 65986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.06e-1

DP
type: SiteQuality
SIO_000300: 1.940587e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 1.003e1

GenotypeQuality
all individuals: 1167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2541
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3164
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4315
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7180
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13147
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2116
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3161
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.813542688910697e-5
allele num: 10190
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: 1.2e-3

VQSLOD
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SIO_000300: -2.472e-1

BaseQRankSum
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SIO_000300: -6.865e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.208e0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 1.940508e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.434e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.515059693351918e-5
allele num: 66004
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.074e1

VQSLOD
type: SiteQuality
SIO_000300: 4.31e-1

DP
type: SiteQuality
SIO_000300: 1.94107e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.572e0

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.57e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6586
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.51336299524804e-5
allele num: 66078
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.968878e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.055e1

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511441613010489e-5
allele num: 66162
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.979403e6

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.66e-1

QD
type: SiteQuality
SIO_000300: 1.143e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.019414837404511e-5
allele num: 66238
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.15e1

DP
type: SiteQuality
SIO_000300: 1.989506e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.48e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66404
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.08198515995621e-5
allele num: 16442
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.007895e6

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

FS
type: SiteQuality
SIO_000300: 8.648e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

QD
type: SiteQuality
SIO_000300: 1.03e1

MQ
type: SiteQuality
SIO_000300: 5.652e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504709741490866e-5
allele num: 66458
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 1.0303e1

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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ClippingRankSum
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DP
type: SiteQuality
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VQSLOD
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BaseQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.948e1

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502900598154438e-5
allele num: 66538
num of homozygotes: 0

South Asian
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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MQ
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MQRankSum
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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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variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
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East Asian
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Latino
type: Population
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

Other
type: Population
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FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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MQ
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
type: SiteQuality
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DP
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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South Asian
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allele count: 0
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num of homozygotes: 0

African
type: Population
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Other
type: Population
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8652
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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