16-4558008-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558008
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558008
    reference: chr 16
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.499C>G
  hgvsp: ENSP00000381595.3:p.Leu167Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.499C>G
  hgvsp: ENSP00000458797.1:p.Leu167Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.499C>G
  hgvsp: ENSP00000391637.1:p.Leu167Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.499C>G
  hgvsp: ENSP00000458592.1:p.Leu167Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.412C>G
  hgvsp: ENSP00000460926.1:p.Leu138Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.499C>G
  hgvsp: ENSP00000459214.1:p.Leu167Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.499C>G
  hgvsp: ENSP00000219700.6:p.Leu167Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.499C>G
  hgvsp: ENSP00000385100.2:p.Leu167Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.499C>G
  hgvsp: ENSP00000394103.3:p.Leu167Val
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu167Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

16-4558014-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558014
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558014
    reference: chr 16
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.505A>G
  hgvsp: ENSP00000385100.2:p.Lys169Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.505A>G
  hgvsp: ENSP00000381595.3:p.Lys169Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.418A>G
  hgvsp: ENSP00000460926.1:p.Lys140Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.505A>G
  hgvsp: ENSP00000394103.3:p.Lys169Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.505A>G
  hgvsp: ENSP00000458797.1:p.Lys169Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.505A>G
  hgvsp: ENSP00000458592.1:p.Lys169Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.505A>G
  hgvsp: ENSP00000219700.6:p.Lys169Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.505A>G
  hgvsp: ENSP00000459214.1:p.Lys169Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.505A>G
  hgvsp: ENSP00000391637.1:p.Lys169Glu
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17013
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys169Glu
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

16-4558015-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558015
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558015
    reference: chr 16
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.506A>T
  hgvsp: ENSP00000391637.1:p.Lys169Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.506A>T
  hgvsp: ENSP00000458592.1:p.Lys169Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.506A>T
  hgvsp: ENSP00000459214.1:p.Lys169Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.506A>T
  hgvsp: ENSP00000381595.3:p.Lys169Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.506A>T
  hgvsp: ENSP00000394103.3:p.Lys169Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.506A>T
  hgvsp: ENSP00000458797.1:p.Lys169Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.506A>T
  hgvsp: ENSP00000385100.2:p.Lys169Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.506A>T
  hgvsp: ENSP00000219700.6:p.Lys169Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.419A>T
  hgvsp: ENSP00000460926.1:p.Lys140Met
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17016
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4254
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4409
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys169Met
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

16-4558018-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558018
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558018
    reference: chr 16
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.509T>C
  hgvsp: ENSP00000381595.3:p.Val170Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.509T>C
  hgvsp: ENSP00000391637.1:p.Val170Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.509T>C
  hgvsp: ENSP00000458797.1:p.Val170Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.422T>C
  hgvsp: ENSP00000460926.1:p.Val141Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.509T>C
  hgvsp: ENSP00000458592.1:p.Val170Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.509T>C
  hgvsp: ENSP00000385100.2:p.Val170Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.509T>C
  hgvsp: ENSP00000459214.1:p.Val170Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.509T>C
  hgvsp: ENSP00000394103.3:p.Val170Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.509T>C
  hgvsp: ENSP00000219700.6:p.Val170Ala
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17010
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12363
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val170Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

16-4558025-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558025
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558025
    reference: chr 16
allele count: 1
allele frequency: 8.25559316436886e-6
allele num: 121130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.516G>A
  hgvsp: ENST00000219700.6:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.516G>A
  hgvsp: ENST00000458134.3:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.516G>A
  hgvsp: ENST00000570445.1:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.516G>A
  hgvsp: ENST00000570646.1:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.429G>A
  hgvsp: ENST00000575120.1:c.429G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.516G>A
  hgvsp: ENST00000414777.1:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.516G>A
  hgvsp: ENST00000398595.3:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.516G>A
  hgvsp: ENST00000575051.1:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.516G>A
  hgvsp: ENST00000406590.2:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7893
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2508
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln172Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

16-4558026-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558026
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558026
    reference: chr 16
allele count: 2
allele frequency: 1.651418568550385e-5
allele num: 121108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.517C>T
  hgvsp: ENSP00000381595.3:p.Arg173Ter
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.517C>T
  hgvsp: ENSP00000219700.6:p.Arg173Ter
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.517C>T
  hgvsp: ENSP00000391637.1:p.Arg173Ter
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.517C>T
  hgvsp: ENSP00000458592.1:p.Arg173Ter
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.430C>T
  hgvsp: ENSP00000460926.1:p.Arg144Ter
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.517C>T
  hgvsp: ENSP00000459214.1:p.Arg173Ter
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.517C>T
  hgvsp: ENSP00000385100.2:p.Arg173Ter
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.517C>T
  hgvsp: ENSP00000458797.1:p.Arg173Ter
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.517C>T
  hgvsp: ENSP00000394103.3:p.Arg173Ter
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4241
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg173Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

16-4558027-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558027
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558027
    reference: chr 16
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.518G>A
  hgvsp: ENSP00000459214.1:p.Arg173Gln
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.518G>A
  hgvsp: ENSP00000394103.3:p.Arg173Gln
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.431G>A
  hgvsp: ENSP00000460926.1:p.Arg144Gln
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.518G>A
  hgvsp: ENSP00000458797.1:p.Arg173Gln
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.518G>A
  hgvsp: ENSP00000458592.1:p.Arg173Gln
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.518G>A
  hgvsp: ENSP00000381595.3:p.Arg173Gln
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.518G>A
  hgvsp: ENSP00000385100.2:p.Arg173Gln
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.518G>A
  hgvsp: ENSP00000219700.6:p.Arg173Gln
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.518G>A
  hgvsp: ENSP00000391637.1:p.Arg173Gln
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19752
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg173Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

16-4558034-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558034
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558034
    reference: chr 16
allele count: 53
allele frequency: 4.374380983823044e-4
allele num: 121160
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.525G>C
  hgvsp: ENST00000570445.1:c.525G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.525G>C
  hgvsp: ENST00000575051.1:c.525G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.525G>C
  hgvsp: ENST00000219700.6:c.525G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.525G>C
  hgvsp: ENST00000406590.2:c.525G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.525G>C
  hgvsp: ENST00000458134.3:c.525G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.525G>C
  hgvsp: ENST00000414777.1:c.525G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.438G>C
  hgvsp: ENST00000575120.1:c.438G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.525G>C
  hgvsp: ENST00000570646.1:c.525G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.525G>C
  hgvsp: ENST00000398595.3:c.525G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 16942
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7322
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13231
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12389
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4154
  bin: 4.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3094
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu175Leu
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

16-4558039-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558039
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558038
    reference: chr 16
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.534delC
  hgvsp: ENSP00000458797.1:p.Ser179AlafsTer28
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.534delC
  hgvsp: ENSP00000394103.3:p.Ser179AlafsTer28
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.534delC
  hgvsp: ENSP00000458592.1:p.Ser179AlafsTer28
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.534delC
  hgvsp: ENSP00000219700.6:p.Ser179AlafsTer28
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.534delC
  hgvsp: ENSP00000381595.3:p.Ser179AlafsTer28
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.534delC
  hgvsp: ENSP00000391637.1:p.Ser179AlafsTer28
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.534delC
  hgvsp: ENSP00000385100.2:p.Ser179AlafsTer28
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.534delC
  hgvsp: ENSP00000459214.1:p.Ser179AlafsTer28
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.447delC
  hgvsp: ENSP00000460926.1:p.Ser150AlafsTer28
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7865
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser179AlafsTer28
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: TC
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

16-4558052-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558052
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558052
    reference: chr 16
allele count: 1
allele frequency: 8.251914444151043e-6
allele num: 121184
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.543G>T
  hgvsp: ENST00000570646.1:c.543G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.543G>T
  hgvsp: ENST00000414777.1:c.543G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.456G>T
  hgvsp: ENST00000575120.1:c.456G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.543G>T
  hgvsp: ENST00000406590.2:c.543G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.543G>T
  hgvsp: ENST00000575051.1:c.543G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.543G>T
  hgvsp: ENST00000398595.3:c.543G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.543G>T
  hgvsp: ENST00000219700.6:c.543G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.543G>T
  hgvsp: ENST00000458134.3:c.543G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.543G>T
  hgvsp: ENST00000570445.1:c.543G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4249
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12162
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly181Gly
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

16-4558053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558053
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558053
    reference: chr 16
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.544G>A
  hgvsp: ENSP00000458797.1:p.Glu182Lys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.544G>A
  hgvsp: ENSP00000391637.1:p.Glu182Lys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.544G>A
  hgvsp: ENSP00000381595.3:p.Glu182Lys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.544G>A
  hgvsp: ENSP00000219700.6:p.Glu182Lys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.544G>A
  hgvsp: ENSP00000459214.1:p.Glu182Lys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.457G>A
  hgvsp: ENSP00000460926.1:p.Glu153Lys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.544G>A
  hgvsp: ENSP00000458592.1:p.Glu182Lys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.544G>A
  hgvsp: ENSP00000385100.2:p.Glu182Lys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.544G>A
  hgvsp: ENSP00000394103.3:p.Glu182Lys
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19476
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu182Lys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

16-4558055-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558055
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558055
    reference: chr 16
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.546A>G
  hgvsp: ENST00000414777.1:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.546A>G
  hgvsp: ENST00000570445.1:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.546A>G
  hgvsp: ENST00000398595.3:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.459A>G
  hgvsp: ENST00000575120.1:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.546A>G
  hgvsp: ENST00000406590.2:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.546A>G
  hgvsp: ENST00000570646.1:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.546A>G
  hgvsp: ENST00000575051.1:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.546A>G
  hgvsp: ENST00000219700.6:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.546A>G
  hgvsp: ENST00000458134.3:c.546A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu182Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-4558064-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558064
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558064
    reference: chr 16
allele count: 310
allele frequency: 2.556996271734468e-3
allele num: 121236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.555G>A
  hgvsp: ENST00000406590.2:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.555G>A
  hgvsp: ENST00000219700.6:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.555G>A
  hgvsp: ENST00000570646.1:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.555G>A
  hgvsp: ENST00000575051.1:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.555G>A
  hgvsp: ENST00000458134.3:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.555G>A
  hgvsp: ENST00000570445.1:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.468G>A
  hgvsp: ENST00000575120.1:c.468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.555G>A
  hgvsp: ENST00000398595.3:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.555G>A
  hgvsp: ENST00000414777.1:c.555G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.5G>A
  hgvsp: ENST00000570622.1:c.5G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 4.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 12410
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16757
  bin: 2.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 3.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 5.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 6.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4202
  bin: 4.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 13008
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln185Gln
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

16-4558064-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558064
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558064
    reference: chr 16
allele count: 4
allele frequency: 3.299350028044475e-5
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.555G>T
  hgvsp: ENSP00000394103.3:p.Gln185His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.468G>T
  hgvsp: ENSP00000460926.1:p.Gln156His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.555G>T
  hgvsp: ENSP00000458592.1:p.Gln185His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.555G>T
  hgvsp: ENSP00000219700.6:p.Gln185His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.555G>T
  hgvsp: ENSP00000385100.2:p.Gln185His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.555G>T
  hgvsp: ENSP00000458797.1:p.Gln185His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.555G>T
  hgvsp: ENSP00000459214.1:p.Gln185His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.5G>T
  hgvsp: ENSP00000459203.1:p.Gln2His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.555G>T
  hgvsp: ENSP00000381595.3:p.Gln185His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.555G>T
  hgvsp: ENSP00000391637.1:p.Gln185His
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4202
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7748
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gln185His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS

16-4558086-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558086
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558086
    reference: chr 16
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.490G>C
  hgvsp: ENSP00000460926.1:p.Asp164His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.577G>C
  hgvsp: ENSP00000391637.1:p.Asp193His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.577G>C
  hgvsp: ENSP00000219700.6:p.Asp193His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.577G>C
  hgvsp: ENSP00000381595.3:p.Asp193His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.577G>C
  hgvsp: ENSP00000394103.3:p.Asp193His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.27G>C
  hgvsp: ENSP00000459203.1:p.Asp10His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.577G>C
  hgvsp: ENSP00000458592.1:p.Asp193His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.577G>C
  hgvsp: ENSP00000458797.1:p.Asp193His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.577G>C
  hgvsp: ENSP00000385100.2:p.Asp193His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.577G>C
  hgvsp: ENSP00000459214.1:p.Asp193His
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp193His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-4558088-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558088
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558088
    reference: chr 16
allele count: 2
allele frequency: 1.649348507339601e-5
allele num: 121260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.29C>G
  hgvsp: ENSP00000459203.1:p.Asp10Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.579C>G
  hgvsp: ENSP00000394103.3:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.579C>G
  hgvsp: ENSP00000458592.1:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.579C>G
  hgvsp: ENSP00000459214.1:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.579C>G
  hgvsp: ENSP00000219700.6:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.579C>G
  hgvsp: ENSP00000381595.3:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.579C>G
  hgvsp: ENSP00000385100.2:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.579C>G
  hgvsp: ENSP00000458797.1:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.492C>G
  hgvsp: ENSP00000460926.1:p.Asp164Glu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.579C>G
  hgvsp: ENSP00000391637.1:p.Asp193Glu
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp193Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-4558090-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558090
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558090
    reference: chr 16
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.581A>G
  hgvsp: ENSP00000458592.1:p.Asn194Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.581A>G
  hgvsp: ENSP00000391637.1:p.Asn194Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.581A>G
  hgvsp: ENSP00000385100.2:p.Asn194Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.494A>G
  hgvsp: ENSP00000460926.1:p.Asn165Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.581A>G
  hgvsp: ENSP00000394103.3:p.Asn194Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.581A>G
  hgvsp: ENSP00000459214.1:p.Asn194Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.31A>G
  hgvsp: ENSP00000459203.1:p.Asn11Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.581A>G
  hgvsp: ENSP00000219700.6:p.Asn194Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.581A>G
  hgvsp: ENSP00000381595.3:p.Asn194Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.581A>G
  hgvsp: ENSP00000458797.1:p.Asn194Ser
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn194Ser
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP

16-4558091-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558091
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558091
    reference: chr 16
allele count: 2
allele frequency: 1.649212501030758e-5
allele num: 121270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.582T>C
  hgvsp: ENST00000219700.6:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.582T>C
  hgvsp: ENST00000570646.1:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.582T>C
  hgvsp: ENST00000458134.3:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.582T>C
  hgvsp: ENST00000398595.3:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.582T>C
  hgvsp: ENST00000406590.2:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.582T>C
  hgvsp: ENST00000570445.1:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.582T>C
  hgvsp: ENST00000414777.1:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.495T>C
  hgvsp: ENST00000575120.1:c.495T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.582T>C
  hgvsp: ENST00000575051.1:c.582T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.32T>C
  hgvsp: ENST00000570622.1:c.32T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn194Asn
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

16-4558093-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558093
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558093
    reference: chr 16
allele count: 3
allele frequency: 2.473941153186436e-5
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.584C>T
  hgvsp: ENSP00000381595.3:p.Ala195Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.584C>T
  hgvsp: ENSP00000391637.1:p.Ala195Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.584C>T
  hgvsp: ENSP00000458592.1:p.Ala195Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.584C>T
  hgvsp: ENSP00000394103.3:p.Ala195Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.584C>T
  hgvsp: ENSP00000458797.1:p.Ala195Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.497C>T
  hgvsp: ENSP00000460926.1:p.Ala166Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.584C>T
  hgvsp: ENSP00000219700.6:p.Ala195Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.584C>T
  hgvsp: ENSP00000459214.1:p.Ala195Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.34C>T
  hgvsp: ENSP00000459203.1:p.Ala12Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.584C>T
  hgvsp: ENSP00000385100.2:p.Ala195Val
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12969
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16748
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12271
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Ala195Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

16-4558105-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558105
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558105
    reference: chr 16
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.46A>G
  hgvsp: ENSP00000459203.1:p.Lys16Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.596A>G
  hgvsp: ENSP00000459214.1:p.Lys199Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.596A>G
  hgvsp: ENSP00000219700.6:p.Lys199Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.596A>G
  hgvsp: ENSP00000458797.1:p.Lys199Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.596A>G
  hgvsp: ENSP00000385100.2:p.Lys199Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.596A>G
  hgvsp: ENSP00000394103.3:p.Lys199Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.596A>G
  hgvsp: ENSP00000381595.3:p.Lys199Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.596A>G
  hgvsp: ENSP00000458592.1:p.Lys199Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.596A>G
  hgvsp: ENSP00000391637.1:p.Lys199Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.509A>G
  hgvsp: ENSP00000460926.1:p.Lys170Arg
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys199Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

16-4558116-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558116
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558116
    reference: chr 16
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.607C>T
  hgvsp: ENSP00000459214.1:p.Arg203Trp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.57C>T
  hgvsp: ENSP00000459203.1:p.Arg20Trp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.607C>T
  hgvsp: ENSP00000458797.1:p.Arg203Trp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.520C>T
  hgvsp: ENSP00000460926.1:p.Arg174Trp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.607C>T
  hgvsp: ENSP00000458592.1:p.Arg203Trp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.607C>T
  hgvsp: ENSP00000385100.2:p.Arg203Trp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.607C>T
  hgvsp: ENSP00000394103.3:p.Arg203Trp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.607C>T
  hgvsp: ENSP00000381595.3:p.Arg203Trp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.607C>T
  hgvsp: ENSP00000219700.6:p.Arg203Trp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.607C>T
  hgvsp: ENSP00000391637.1:p.Arg203Trp
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg203Trp
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-4558122-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558122
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558122
    reference: chr 16
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.613A>C
  hgvsp: ENST00000219700.6:c.613A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.613A>C
  hgvsp: ENST00000406590.2:c.613A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.613A>C
  hgvsp: ENST00000398595.3:c.613A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.613A>C
  hgvsp: ENST00000575051.1:c.613A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.613A>C
  hgvsp: ENST00000570445.1:c.613A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.526A>C
  hgvsp: ENST00000575120.1:c.526A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.613A>C
  hgvsp: ENST00000458134.3:c.613A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.613A>C
  hgvsp: ENST00000570646.1:c.613A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.613A>C
  hgvsp: ENST00000414777.1:c.613A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.63A>C
  hgvsp: ENST00000570622.1:c.63A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16948
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg205Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP

16-4558131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558131
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558131
    reference: chr 16
allele count: 3
allele frequency: 2.475982965237199e-5
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.622G>A
  hgvsp: ENSP00000385100.2:p.Ala208Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.622G>A
  hgvsp: ENSP00000381595.3:p.Ala208Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.535G>A
  hgvsp: ENSP00000460926.1:p.Ala179Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.622G>A
  hgvsp: ENSP00000458592.1:p.Ala208Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.622G>A
  hgvsp: ENSP00000459214.1:p.Ala208Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.622G>A
  hgvsp: ENSP00000458797.1:p.Ala208Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.72G>A
  hgvsp: ENSP00000459203.1:p.Ala25Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.622G>A
  hgvsp: ENSP00000394103.3:p.Ala208Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.622G>A
  hgvsp: ENSP00000219700.6:p.Ala208Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.622G>A
  hgvsp: ENSP00000391637.1:p.Ala208Thr
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala208Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

16-4558131-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558131
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558131
    reference: chr 16
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.622G>T
  hgvsp: ENSP00000394103.3:p.Ala208Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.622G>T
  hgvsp: ENSP00000458592.1:p.Ala208Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.622G>T
  hgvsp: ENSP00000219700.6:p.Ala208Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.622G>T
  hgvsp: ENSP00000458797.1:p.Ala208Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.622G>T
  hgvsp: ENSP00000459214.1:p.Ala208Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.535G>T
  hgvsp: ENSP00000460926.1:p.Ala179Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.622G>T
  hgvsp: ENSP00000381595.3:p.Ala208Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.622G>T
  hgvsp: ENSP00000385100.2:p.Ala208Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.622G>T
  hgvsp: ENSP00000391637.1:p.Ala208Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.72G>T
  hgvsp: ENSP00000459203.1:p.Ala25Ser
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala208Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ

16-4558136-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558136
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558136
    reference: chr 16
allele count: 5
allele frequency: 4.128682785044259e-5
allele num: 121104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.540G>A
  hgvsp: ENST00000575120.1:c.540G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.627G>A
  hgvsp: ENST00000219700.6:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.627G>A
  hgvsp: ENST00000570646.1:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.627G>A
  hgvsp: ENST00000570445.1:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.627G>A
  hgvsp: ENST00000414777.1:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.627G>A
  hgvsp: ENST00000398595.3:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.627G>A
  hgvsp: ENST00000406590.2:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.627G>A
  hgvsp: ENST00000575051.1:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.627G>A
  hgvsp: ENST00000458134.3:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.77G>A
  hgvsp: ENST00000570622.1:c.77G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu209Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

16-4558145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558145
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558145
    reference: chr 16
allele count: 2
allele frequency: 1.655135886656295e-5
allele num: 120836
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.636C>T
  hgvsp: ENST00000406590.2:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.636C>T
  hgvsp: ENST00000458134.3:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.636C>T
  hgvsp: ENST00000570646.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.636C>T
  hgvsp: ENST00000575051.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.636C>T
  hgvsp: ENST00000414777.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.636C>T
  hgvsp: ENST00000398595.3:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.636C>T
  hgvsp: ENST00000570445.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.636C>T
  hgvsp: ENST00000219700.6:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.549C>T
  hgvsp: ENST00000575120.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.86C>T
  hgvsp: ENST00000570622.1:c.86C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn212Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP

16-4558150-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558150
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558150
    reference: chr 16
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.641A>G
  hgvsp: ENSP00000385100.2:p.Lys214Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.554A>G
  hgvsp: ENSP00000460926.1:p.Lys185Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.641A>G
  hgvsp: ENSP00000458592.1:p.Lys214Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.641A>G
  hgvsp: ENSP00000458797.1:p.Lys214Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.91A>G
  hgvsp: ENSP00000459203.1:p.Lys31Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.641A>G
  hgvsp: ENSP00000391637.1:p.Lys214Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.641A>G
  hgvsp: ENSP00000394103.3:p.Lys214Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.641A>G
  hgvsp: ENSP00000459214.1:p.Lys214Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.641A>G
  hgvsp: ENSP00000381595.3:p.Lys214Arg
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.641A>G
  hgvsp: ENSP00000219700.6:p.Lys214Arg
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys214Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

16-4558166-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558166
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558166
    reference: chr 16
allele count: 9
allele frequency: 7.527349369375398e-5
allele num: 119564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.657C>T
  hgvsp: ENST00000219700.6:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.570C>T
  hgvsp: ENST00000575120.1:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.657C>T
  hgvsp: ENST00000570445.1:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.657C>T
  hgvsp: ENST00000570646.1:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.657C>T
  hgvsp: ENST00000458134.3:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.657C>T
  hgvsp: ENST00000398595.3:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.657C>T
  hgvsp: ENST00000575051.1:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.657C>T
  hgvsp: ENST00000406590.2:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.107C>T
  hgvsp: ENST00000570622.1:c.107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.657C>T
  hgvsp: ENST00000414777.1:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11524
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile219Ile
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

16-4558167-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558167
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558167
    reference: chr 16
allele count: 1
allele frequency: 8.367920739054759e-6
allele num: 119504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.658G>A
  hgvsp: ENSP00000458592.1:p.Val220Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.108G>A
  hgvsp: ENSP00000459203.1:p.Val37Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.658G>A
  hgvsp: ENSP00000459214.1:p.Val220Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.658G>A
  hgvsp: ENSP00000458797.1:p.Val220Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.658G>A
  hgvsp: ENSP00000385100.2:p.Val220Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.658G>A
  hgvsp: ENSP00000381595.3:p.Val220Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.571G>A
  hgvsp: ENSP00000460926.1:p.Val191Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.658G>A
  hgvsp: ENSP00000394103.3:p.Val220Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.658G>A
  hgvsp: ENSP00000391637.1:p.Val220Met
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.658G>A
  hgvsp: ENSP00000219700.6:p.Val220Met
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val220Met
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

16-4558172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558172
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558172
    reference: chr 16
allele count: 1
allele frequency: 8.396446623788812e-6
allele num: 119098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.663G>A
  hgvsp: ENST00000458134.3:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.663G>A
  hgvsp: ENST00000219700.6:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.113G>A
  hgvsp: ENST00000570622.1:c.113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.576G>A
  hgvsp: ENST00000575120.1:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.663G>A
  hgvsp: ENST00000575051.1:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.663G>A
  hgvsp: ENST00000398595.3:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.663G>A
  hgvsp: ENST00000570646.1:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.663G>A
  hgvsp: ENST00000406590.2:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.663G>A
  hgvsp: ENST00000570445.1:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.663G>A
  hgvsp: ENST00000414777.1:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu221Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/16-4558174-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558174
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558174
    reference: chr 16
allele count: 1
allele frequency: 8.43113449345744e-6
allele num: 118608
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.665A>C
  hgvsp: ENSP00000458592.1:p.Glu222Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.665A>C
  hgvsp: ENSP00000394103.3:p.Glu222Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.578A>C
  hgvsp: ENSP00000460926.1:p.Glu193Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.665A>C
  hgvsp: ENSP00000385100.2:p.Glu222Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.665A>C
  hgvsp: ENSP00000459214.1:p.Glu222Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.115A>C
  hgvsp: ENSP00000459203.1:p.Glu39Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.665A>C
  hgvsp: ENSP00000219700.6:p.Glu222Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.665A>C
  hgvsp: ENSP00000458797.1:p.Glu222Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.665A>C
  hgvsp: ENSP00000381595.3:p.Glu222Ala
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.665A>C
  hgvsp: ENSP00000391637.1:p.Glu222Ala
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu222Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

16-4558179-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558179
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558179
    reference: chr 16
allele count: 1
allele frequency: 8.455658526686058e-6
allele num: 118264
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.670A>G
  hgvsp: ENSP00000459214.1:p.Asn224Asp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.670A>G
  hgvsp: ENSP00000381595.3:p.Asn224Asp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.670A>G
  hgvsp: ENSP00000385100.2:p.Asn224Asp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.120A>G
  hgvsp: ENSP00000459203.1:p.Asn41Asp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.670A>G
  hgvsp: ENSP00000219700.6:p.Asn224Asp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.670A>G
  hgvsp: ENSP00000458592.1:p.Asn224Asp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.670A>G
  hgvsp: ENSP00000391637.1:p.Asn224Asp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.583A>G
  hgvsp: ENSP00000460926.1:p.Asn195Asp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.670A>G
  hgvsp: ENSP00000458797.1:p.Asn224Asp
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.670A>G
  hgvsp: ENSP00000394103.3:p.Asn224Asp
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn224Asp
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

16-4558180-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558180
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558180
    reference: chr 16
allele count: 1
allele frequency: 8.463817181548878e-6
allele num: 118150
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.671A>G
  hgvsp: ENSP00000394103.3:p.Asn224Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.671A>G
  hgvsp: ENSP00000219700.6:p.Asn224Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.671A>G
  hgvsp: ENSP00000385100.2:p.Asn224Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.671A>G
  hgvsp: ENSP00000459214.1:p.Asn224Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.671A>G
  hgvsp: ENSP00000458592.1:p.Asn224Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.584A>G
  hgvsp: ENSP00000460926.1:p.Asn195Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.671A>G
  hgvsp: ENSP00000458797.1:p.Asn224Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.121A>G
  hgvsp: ENSP00000459203.1:p.Asn41Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.671A>G
  hgvsp: ENSP00000381595.3:p.Asn224Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.671A>G
  hgvsp: ENSP00000391637.1:p.Asn224Ser
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10631
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4689
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asn224Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

16-4558195-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558195
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558195
    reference: chr 16
allele count: 1
allele frequency: 8.572947207791094e-6
allele num: 116646
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.686A>G
  hgvsp: ENSP00000381595.3:p.Tyr229Cys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.136A>G
  hgvsp: ENSP00000459203.1:p.Tyr46Cys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458592
  ensembl transcript: ENST00000570445
  gene symbol: HMOX2
  hgvsc: ENST00000570445.1:c.686A>G
  hgvsp: ENSP00000458592.1:p.Tyr229Cys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.686A>G
  hgvsp: ENSP00000385100.2:p.Tyr229Cys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.686A>G
  hgvsp: ENSP00000219700.6:p.Tyr229Cys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.686A>G
  hgvsp: ENSP00000459214.1:p.Tyr229Cys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.686A>G
  hgvsp: ENSP00000394103.3:p.Tyr229Cys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.686A>G
  hgvsp: ENSP00000458797.1:p.Tyr229Cys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.686A>G
  hgvsp: ENSP00000391637.1:p.Tyr229Cys
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.599A>G
  hgvsp: ENSP00000460926.1:p.Tyr200Cys
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr229Cys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

16-4558212-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558212
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558212
    reference: chr 16
allele count: 2
allele frequency: 1.743466359816587e-5
allele num: 114714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+7T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+7T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+7T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+7T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+7T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+7T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+7T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+7T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+7T>C
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12843
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2611
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14655
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 925
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
hgvs: c.696+7T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-4558212-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558212
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558212
    reference: chr 16
allele count: 17
allele frequency: 1.481946405844099e-4
allele num: 114714
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+7T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+7T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+7T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+7T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+7T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+7T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+7T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+7T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+7T>G
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3572
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7497
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 3.25e1
  variant carriers: 0
hgvs: c.696+7T>G
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

16-4558213-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558213
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558213
    reference: chr 16
allele count: 2
allele frequency: 1.745139785696834e-5
allele num: 114604
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+8T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+8T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+8T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+8T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+8T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+8T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+8T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+8T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+8T>G
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14633
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2610
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
hgvs: c.696+8T>G
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

16-4558214-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558214
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558214
    reference: chr 16
allele count: 221
allele frequency: 1.929659122659961e-3
allele num: 114528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+9G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+9G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+9G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+9G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+9G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+9G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+9G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+9G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+9G>A
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 7548
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 12814
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15012
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4372
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4675
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum

16-4558214-G-GGGGGCTGCCAGCTGCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558214
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558230
    reference: chr 16
allele count: 3
allele frequency: 2.619446772841576e-5
allele num: 114528
alternate allele: GGGGGCTGCCAGCTGCT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7548
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4372
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

16-4558218-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558218
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558218
    reference: chr 16
allele count: 1
allele frequency: 8.801887124599515e-6
allele num: 113612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+13G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+13G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+13G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+13G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+13G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+13G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+13G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+13G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+13G>A
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2607
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7456
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2909
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-4558233-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558233
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558233
    reference: chr 16
allele count: 1
allele frequency: 8.94470384085583e-6
allele num: 111798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+28G>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+28G>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+28G>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+28G>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+28G>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+28G>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+28G>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+28G>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+28G>C
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12793
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1881
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2285
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4680
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

16-4558233-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558233
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558233
    reference: chr 16
allele count: 2
allele frequency: 1.788940768171166e-5
allele num: 111798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+28G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+28G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+28G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+28G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+28G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+28G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+28G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+28G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+28G>T
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12793
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1881
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4381
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7421
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4680
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-4558235-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558235
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558235
    reference: chr 16
allele count: 1
allele frequency: 8.94774516821761e-6
allele num: 111760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+30C>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+30C>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+30C>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+30C>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+30C>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+30C>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+30C>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+30C>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+30C>G
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

16-4558235-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558235
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558235
    reference: chr 16
allele count: 1
allele frequency: 8.94774516821761e-6
allele num: 111760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+30C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+30C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+30C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+30C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+30C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+30C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+30C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+30C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+30C>T
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12469
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4384
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4682
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2290
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

16-4558254-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558254
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558254
    reference: chr 16
allele count: 1
allele frequency: 9.013068949977467e-6
allele num: 110950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+49C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+49C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+49C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+49C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+49C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+49C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+49C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+49C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+49C>T
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5551
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4379
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

16-4558255-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558255
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558255
    reference: chr 16
allele count: 3
allele frequency: 2.703141049899984e-5
allele num: 110982
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+50A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+50A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+50A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+50A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+50A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+50A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+50A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+50A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+50A>G
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4378
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

16-4558257-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4558257
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4558257
    reference: chr 16
allele count: 2
allele frequency: 1.802581296416468e-5
allele num: 110952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.696+52T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.696+52T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.609+52T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.696+52T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.696+52T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.696+52T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.696+52T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.146+52T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.696+52T>C
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4328
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12480
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

16-4559364-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559364
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559365
    reference: chr 16
allele count: 1
allele frequency: 8.531258531258532e-6
allele num: 117216
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.697-49_697-48insG
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.697-49_697-48insG
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.697-49_697-48insG
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.697-49_697-48insG
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.697-49_697-48insG
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.697-49_697-48insG
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.147-49_147-48insG
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.610-49_610-48insG
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.697-49_697-48insG
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1644
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

16-4559366-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559366
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559366
    reference: chr 16
allele count: 1
allele frequency: 8.511942254983741e-6
allele num: 117482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.697-47A>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.697-47A>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.697-47A>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.610-47A>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.697-47A>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.697-47A>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.147-47A>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.697-47A>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.697-47A>T
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39051
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2327
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

16-4559368-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559368
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559368
    reference: chr 16
allele count: 2
allele frequency: 1.763201974786212e-5
allele num: 113430
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.697-45T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.147-45T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.610-45T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.697-45T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.697-45T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.697-45T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.697-45T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.697-45T>C
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.697-45T>C
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7002
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2197
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-4559368-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559368
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559368
    reference: chr 16
allele count: 4
allele frequency: 3.526403949572424e-5
allele num: 113430
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.697-45T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.697-45T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.610-45T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.697-45T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.697-45T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.697-45T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.147-45T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.697-45T>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.697-45T>G
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7002
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2197
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-4559377-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559377
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559377
    reference: chr 16
allele count: 1
allele frequency: 8.378296859814337e-6
allele num: 119356
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.697-36C>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.697-36C>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.610-36C>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.697-36C>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.147-36C>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.697-36C>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.697-36C>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.697-36C>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.697-36C>A
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43249
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum

16-4559381-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559381
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559381
    reference: chr 16
allele count: 1
allele frequency: 8.350451759440186e-6
allele num: 119754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.697-32A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.697-32A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.697-32A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.697-32A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.697-32A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.697-32A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.147-32A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.697-32A>G
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.610-32A>G
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

16-4559388-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559388
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559388
    reference: chr 16
allele count: 4
allele frequency: 3.329892444474044e-5
allele num: 120124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.697-25C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.697-25C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.697-25C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.697-25C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.697-25C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.697-25C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.697-25C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.147-25C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.610-25C>T
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

16-4559394-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559394
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559394
    reference: chr 16
allele count: 1
allele frequency: 8.305233958440609e-6
allele num: 120406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.697-19C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.697-19C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.610-19C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.697-19C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.697-19C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.697-19C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.697-19C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.147-19C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.697-19C>T
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44807
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

16-4559395-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559395
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559395
    reference: chr 16
allele count: 4
allele frequency: 3.319502074688797e-5
allele num: 120500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.697-18G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.697-18G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.697-18G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.697-18G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.610-18G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.697-18G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.697-18G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.697-18G>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.147-18G>T
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

16-4559406-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559406
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559406
    reference: chr 16
allele count: 4
allele frequency: 3.309450134860093e-5
allele num: 120866
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.697-7C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.697-7C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.697-7C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.697-7C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.697-7C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.147-7C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.697-7C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.610-7C>T
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.697-7C>T
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45375
  bin: 6.25e1
  variant carriers: 0
hgvs: c.697-7C>T
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-4559409-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559409
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559409
    reference: chr 16
allele count: 4
allele frequency: 3.307206402751596e-5
allele num: 120948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.697-4G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.697-4G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.697-4G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.697-4G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.697-4G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.610-4G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.697-4G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.147-4G>A
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.697-4G>A
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2111
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
hgvs: c.697-4G>A
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

16-4559416-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559416
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559416
    reference: chr 16
allele count: 2
allele frequency: 1.651473114017704e-5
allele num: 121104
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.700T>C
  hgvsp: ENSP00000459214.1:p.Phe234Leu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.700T>C
  hgvsp: ENSP00000458797.1:p.Phe234Leu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.700T>C
  hgvsp: ENSP00000381595.3:p.Phe234Leu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.613T>C
  hgvsp: ENSP00000460926.1:p.Phe205Leu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.700T>C
  hgvsp: ENSP00000394103.3:p.Phe234Leu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.700T>C
  hgvsp: ENSP00000385100.2:p.Phe234Leu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.700T>C
  hgvsp: ENSP00000219700.6:p.Phe234Leu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.150T>C
  hgvsp: ENSP00000459203.1:p.Phe51Leu
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.700T>C
  hgvsp: ENSP00000391637.1:p.Phe234Leu
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe234Leu
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

16-4559416-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559416
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559416
    reference: chr 16
allele count: 1
allele frequency: 8.257365570088519e-6
allele num: 121104
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.613T>G
  hgvsp: ENSP00000460926.1:p.Phe205Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.700T>G
  hgvsp: ENSP00000381595.3:p.Phe234Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.700T>G
  hgvsp: ENSP00000391637.1:p.Phe234Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.700T>G
  hgvsp: ENSP00000219700.6:p.Phe234Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.700T>G
  hgvsp: ENSP00000394103.3:p.Phe234Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.700T>G
  hgvsp: ENSP00000385100.2:p.Phe234Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.700T>G
  hgvsp: ENSP00000458797.1:p.Phe234Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.150T>G
  hgvsp: ENSP00000459203.1:p.Phe51Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.700T>G
  hgvsp: ENSP00000459214.1:p.Phe234Val
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe234Val
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/16-4559419-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559419
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559419
    reference: chr 16
allele count: 1
allele frequency: 8.255047961828658e-6
allele num: 121138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.703A>C
  hgvsp: ENSP00000219700.6:p.Asn235His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.703A>C
  hgvsp: ENSP00000391637.1:p.Asn235His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.703A>C
  hgvsp: ENSP00000394103.3:p.Asn235His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.616A>C
  hgvsp: ENSP00000460926.1:p.Asn206His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.703A>C
  hgvsp: ENSP00000458797.1:p.Asn235His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.703A>C
  hgvsp: ENSP00000459214.1:p.Asn235His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.703A>C
  hgvsp: ENSP00000385100.2:p.Asn235His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.703A>C
  hgvsp: ENSP00000381595.3:p.Asn235His
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.153A>C
  hgvsp: ENSP00000459203.1:p.Asn52His
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn235His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ

16-4559420-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559420
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559420
    reference: chr 16
allele count: 4
allele frequency: 3.301801132517788e-5
allele num: 121146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.704A>G
  hgvsp: ENSP00000385100.2:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.704A>G
  hgvsp: ENSP00000394103.3:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.704A>G
  hgvsp: ENSP00000459214.1:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.154A>G
  hgvsp: ENSP00000459203.1:p.Asn52Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.704A>G
  hgvsp: ENSP00000391637.1:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.617A>G
  hgvsp: ENSP00000460926.1:p.Asn206Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.704A>G
  hgvsp: ENSP00000219700.6:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.704A>G
  hgvsp: ENSP00000458797.1:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.704A>G
  hgvsp: ENSP00000381595.3:p.Asn235Ser
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn235Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-4559421-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559421
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559421
    reference: chr 16
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.618T>C
  hgvsp: ENST00000575120.1:c.618T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.155T>C
  hgvsp: ENST00000570622.1:c.155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.705T>C
  hgvsp: ENST00000458134.3:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.705T>C
  hgvsp: ENST00000406590.2:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.705T>C
  hgvsp: ENST00000414777.1:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.705T>C
  hgvsp: ENST00000398595.3:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.705T>C
  hgvsp: ENST00000570646.1:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.705T>C
  hgvsp: ENST00000575051.1:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.705T>C
  hgvsp: ENST00000219700.6:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn235Asn
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum

16-4559429-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559429
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559429
    reference: chr 16
allele count: 4
allele frequency: 3.299948850792813e-5
allele num: 121214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.713A>T
  hgvsp: ENSP00000391637.1:p.Asp238Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.626A>T
  hgvsp: ENSP00000460926.1:p.Asp209Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.713A>T
  hgvsp: ENSP00000394103.3:p.Asp238Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.163A>T
  hgvsp: ENSP00000459203.1:p.Asp55Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.713A>T
  hgvsp: ENSP00000219700.6:p.Asp238Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.713A>T
  hgvsp: ENSP00000381595.3:p.Asp238Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.713A>T
  hgvsp: ENSP00000459214.1:p.Asp238Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000458797
  ensembl transcript: ENST00000575051
  gene symbol: HMOX2
  hgvsc: ENST00000575051.1:c.713A>T
  hgvsp: ENSP00000458797.1:p.Asp238Val
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.713A>T
  hgvsp: ENSP00000385100.2:p.Asp238Val
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31263
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp238Val
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

16-4559434-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559434
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559434
    reference: chr 16
allele count: 88
allele frequency: 7.257492536328698e-4
allele num: 121254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.718G>C
  hgvsp: ENSP00000394103.3:p.Ala240Pro
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.631G>C
  hgvsp: ENSP00000460926.1:p.Ala211Pro
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.718G>C
  hgvsp: ENSP00000385100.2:p.Ala240Pro
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.718G>C
  hgvsp: ENSP00000459214.1:p.Ala240Pro
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.718G>C
  hgvsp: ENSP00000219700.6:p.Ala240Pro
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.168G>C
  hgvsp: ENSP00000459203.1:p.Ala57Pro
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.718G>C
  hgvsp: ENSP00000381595.3:p.Ala240Pro
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.718G>C
  hgvsp: ENSP00000391637.1:p.Ala240Pro
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9910
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16405
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 9.75e1
  variant carriers: 88
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala240Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

16-4559436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559436
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559436
    reference: chr 16
allele count: 2
allele frequency: 1.649103712132456e-5
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.720C>T
  hgvsp: ENST00000398595.3:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.170C>T
  hgvsp: ENST00000570622.1:c.170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.720C>T
  hgvsp: ENST00000219700.6:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.720C>T
  hgvsp: ENST00000570646.1:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.720C>T
  hgvsp: ENST00000406590.2:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.720C>T
  hgvsp: ENST00000458134.3:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.720C>T
  hgvsp: ENST00000414777.1:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.633C>T
  hgvsp: ENST00000575120.1:c.633C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala240Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

16-4559441-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559441
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559441
    reference: chr 16
allele count: 2
allele frequency: 1.648750247312537e-5
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.725C>T
  hgvsp: ENSP00000219700.6:p.Ser242Phe
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.725C>T
  hgvsp: ENSP00000385100.2:p.Ser242Phe
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.725C>T
  hgvsp: ENSP00000394103.3:p.Ser242Phe
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.725C>T
  hgvsp: ENSP00000391637.1:p.Ser242Phe
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.725C>T
  hgvsp: ENSP00000381595.3:p.Ser242Phe
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.638C>T
  hgvsp: ENSP00000460926.1:p.Ser213Phe
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.175C>T
  hgvsp: ENSP00000459203.1:p.Ser59Phe
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.725C>T
  hgvsp: ENSP00000459214.1:p.Ser242Phe
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2143
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser242Phe
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ

16-4559442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559442
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559442
    reference: chr 16
allele count: 2
allele frequency: 1.64866870002473e-5
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.639C>T
  hgvsp: ENST00000575120.1:c.639C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.726C>T
  hgvsp: ENST00000398595.3:c.726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.726C>T
  hgvsp: ENST00000458134.3:c.726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.726C>T
  hgvsp: ENST00000414777.1:c.726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.726C>T
  hgvsp: ENST00000570646.1:c.726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.726C>T
  hgvsp: ENST00000406590.2:c.726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.176C>T
  hgvsp: ENST00000570622.1:c.176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.726C>T
  hgvsp: ENST00000219700.6:c.726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8576
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser242Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum

16-4559445-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559445
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559445
    reference: chr 16
allele count: 2
allele frequency: 1.648451280022419e-5
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.729A>G
  hgvsp: ENST00000219700.6:c.729A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.729A>G
  hgvsp: ENST00000414777.1:c.729A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.729A>G
  hgvsp: ENST00000458134.3:c.729A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.729A>G
  hgvsp: ENST00000406590.2:c.729A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.729A>G
  hgvsp: ENST00000398595.3:c.729A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.642A>G
  hgvsp: ENST00000575120.1:c.642A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.729A>G
  hgvsp: ENST00000570646.1:c.729A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.179A>G
  hgvsp: ENST00000570622.1:c.179A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9927
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr243Thr
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

16-4559449-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4559449
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4559449
    reference: chr 16
allele count: 5
allele frequency: 4.120788554097712e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000394103
  ensembl transcript: ENST00000458134
  gene symbol: HMOX2
  hgvsc: ENST00000458134.3:c.733G>A
  hgvsp: ENSP00000394103.3:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000391637
  ensembl transcript: ENST00000414777
  gene symbol: HMOX2
  hgvsc: ENST00000414777.1:c.733G>A
  hgvsp: ENSP00000391637.1:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000219700
  ensembl transcript: ENST00000219700
  gene symbol: HMOX2
  hgvsc: ENST00000219700.6:c.733G>A
  hgvsp: ENSP00000219700.6:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000385100
  ensembl transcript: ENST00000406590
  gene symbol: HMOX2
  hgvsc: ENST00000406590.2:c.733G>A
  hgvsp: ENSP00000385100.2:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000460926
  ensembl transcript: ENST00000575120
  gene symbol: HMOX2
  hgvsc: ENST00000575120.1:c.646G>A
  hgvsp: ENSP00000460926.1:p.Ala216Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459214
  ensembl transcript: ENST00000570646
  gene symbol: HMOX2
  hgvsc: ENST00000570646.1:c.733G>A
  hgvsp: ENSP00000459214.1:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000459203
  ensembl transcript: ENST00000570622
  gene symbol: HMOX2
  hgvsc: ENST00000570622.1:c.183G>A
  hgvsp: ENSP00000459203.1:p.Ala62Thr
  variant of: http://identifiers.org/hgnc/5014
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000103415
  ensembl protein: ENSP00000381595
  ensembl transcript: ENST00000398595
  gene symbol: HMOX2
  hgvsc: ENST00000398595.3:c.733G>A
  hgvsp: ENSP00000381595.3:p.Ala245Thr
  variant of: http://identifiers.org/hgnc/5014
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala245Thr
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 12145
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 167
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4250
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4411
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2502
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19812
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5291
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3096
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7880
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66524
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.23e-1

QD
type: SiteQuality
SIO_000300: 9.66e0

MQRankSum
type: SiteQuality
SIO_000300: 8.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.183e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 6.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.921509e6

GenotypeQuality
all individuals: 7886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12147
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 209
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2504
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4411
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19736
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 357
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5301
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4247
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3095
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

Other
type: Population
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: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502810255177181e-5
allele num: 66542
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.682e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

DP
type: SiteQuality
SIO_000300: 1.921412e6

MQRankSum
type: SiteQuality
SIO_000300: -1.525e0

QD
type: SiteQuality
SIO_000300: 1.142e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.16e-1

MQ
type: SiteQuality
SIO_000300: 5.717e1

VQSLOD
type: SiteQuality
SIO_000300: -1.413e0

GenotypeQuality
all individuals: 19714
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 159
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7889
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 141
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5301
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12149
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 173
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3096
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.199e0

DP
type: SiteQuality
SIO_000300: 1.921388e6

MQ
type: SiteQuality
SIO_000300: 5.717e1

QD
type: SiteQuality
SIO_000300: 1.142e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.623e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.09e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.274e0

GenotypeQuality
all individuals: 176
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7862
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4247
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3096
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5298
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19656
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 175
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2506
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12148
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 169
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
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: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.142e1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 1.623e0

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.783e0

DP
type: SiteQuality
SIO_000300: 1.921219e6

MQ
type: SiteQuality
SIO_000300: 5.717e1

VQSLOD
type: SiteQuality
SIO_000300: -1.292e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

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

East Asian
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allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66556
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.921219e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.668e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.21e-1

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.00543984612148e-5
allele num: 66546
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.16e0

MQ
type: SiteQuality
SIO_000300: 5.908e1

FS
type: SiteQuality
SIO_000300: 2.126e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.921847e6

VQSLOD
type: SiteQuality
SIO_000300: 1.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

QD
type: SiteQuality
SIO_000300: 1.097e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.07e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.43e1

FS
type: SiteQuality
SIO_000300: 2.063e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

DP
type: SiteQuality
SIO_000300: 1.921768e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.182e0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.467406380027739e-4
allele num: 8652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 20
allele frequency: 3.033980582524272e-3
allele num: 6592
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: 30
allele frequency: 4.506263706552108e-4
allele num: 66574
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.923291e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.57e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

QD
type: SiteQuality
SIO_000300: 1.5e1

GenotypeQuality
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variant carriers: 1

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

Latino
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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: 66572
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

QD
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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MQRankSum
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FS
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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SIO_000300: -3.36e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501501501501501e-5
allele num: 66600
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 902
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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African
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South Asian
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QD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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MQ
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VQSLOD
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501501501501501e-5
allele num: 66600
num of homozygotes: 0

East Asian
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Other
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South Asian
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
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MQRankSum
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QD
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.43e0

VQSLOD
type: SiteQuality
SIO_000300: -1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
all individuals: 154
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 237
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3097
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18986
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 281
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4432
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5279
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12408
bin: 9.75e1
variant carriers: 308

GenotypeQuality
all individuals: 368
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7748
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 270
allele frequency: 4.052107095689758e-3
allele num: 66632
num of homozygotes: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 8.667180277349769e-4
allele num: 10384
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.060606060606061e-3
allele num: 6600
num of homozygotes: 0

Latino
type: Population
allele count: 18
allele frequency: 1.557902025272633e-3
allele num: 11554
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

QD
type: SiteQuality
SIO_000300: 1.371e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

DP
type: SiteQuality
SIO_000300: 1.92885e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.955e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

GenotypeQuality
all individuals: 224
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4432
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18986
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5279
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 2504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12408
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 224
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3097
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 7.25e1
variant carriers: 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: 4.502341217433065e-5
allele num: 66632
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

QD
type: SiteQuality
SIO_000300: 1.371e1

VQSLOD
type: SiteQuality
SIO_000300: 6.15e0

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.955e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.92885e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 4328
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3119
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variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 4511
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variant carriers: 0

GenotypeQuality
all individuals: 208
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variant carriers: 0

GenotypeQuality
all individuals: 7802
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variant carriers: 0

GenotypeQuality
all individuals: 226
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variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.25e1
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GenotypeQuality
all individuals: 2539
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 19220
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variant carriers: 0

GenotypeQuality
all individuals: 132
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variant carriers: 0

GenotypeQuality
all individuals: 5378
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12260
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 5.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.26e0

FS
type: SiteQuality
SIO_000300: 2.217e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

QD
type: SiteQuality
SIO_000300: 1.686e1

DP
type: SiteQuality
SIO_000300: 1.930807e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.96e-1

GenotypeQuality
all individuals: 4516
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18900
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 5385
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4337
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12265
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
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: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.474e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

DP
type: SiteQuality
SIO_000300: 1.93149e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.3e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.28e-1

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

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
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variant carriers: 0

GenotypeQuality
all individuals: 19247
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variant carriers: 0

GenotypeQuality
all individuals: 202
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 5404
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variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4531
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12267
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7851
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

FS
type: SiteQuality
SIO_000300: 5.818e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

DP
type: SiteQuality
SIO_000300: 1.932005e6

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

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4358
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variant carriers: 0

GenotypeQuality
all individuals: 130
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 4535
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variant carriers: 0

GenotypeQuality
all individuals: 5406
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12268
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3131
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7850
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.932223e6

QD
type: SiteQuality
SIO_000300: 1.259e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.282e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.72e-1

GenotypeQuality
all individuals: 4536
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4357
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 3130
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GenotypeQuality
all individuals: 221
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 19086
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GenotypeQuality
all individuals: 235
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variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 4.75e1
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GenotypeQuality
all individuals: 123
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 3.25e1
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GenotypeQuality
all individuals: 7829
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2552
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5405
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500990217847926e-5
allele num: 66652
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.623e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.186e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

DP
type: SiteQuality
SIO_000300: 1.933519e6

QD
type: SiteQuality
SIO_000300: 1.293e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

GenotypeQuality
all individuals: 19351
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variant carriers: 0

GenotypeQuality
all individuals: 135
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GenotypeQuality
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GenotypeQuality
all individuals: 91
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 119
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GenotypeQuality
all individuals: 12296
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variant carriers: 1

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 7889
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variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.25e1
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GenotypeQuality
all individuals: 4596
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variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.25e1
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GenotypeQuality
all individuals: 3142
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5491
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 3.75e1
variant carriers: 0

Latino
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allele count: 0
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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ClippingRankSum
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QD
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FS
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BaseQRankSum
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InbreedingCoeff
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DP
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SIO_000300: 1.937877e6

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

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

East Asian
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ClippingRankSum
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VQSLOD
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QD
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FS
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DP
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BaseQRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.002191599867904e-5
allele num: 66618
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.092360180333861e-5
allele num: 16414
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 2.0e-4

ClippingRankSum
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MQRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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FS
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SIO_000300: 9.641999999999999e0

MQ
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SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.328e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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Latino
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allele frequency: 3.457814661134163e-4
allele num: 11568
num of homozygotes: 0

African
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European (Non-Finnish)
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allele frequency: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

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

East Asian
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South Asian
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Latino
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African
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Other
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European (Non-Finnish)
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allele num: 66484
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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BaseQRankSum
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DP
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FS
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MQ
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66166
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

South Asian
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allele count: 8
allele frequency: 5.221932114882506e-4
allele num: 15320
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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QD
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SIO_000300: 1.15e1

InbreedingCoeff
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MQRankSum
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BaseQRankSum
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SIO_000300: -1.59e-1

FS
type: SiteQuality
SIO_000300: 5.21e-1

ClippingRankSum
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SIO_000300: 7.6e-2

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

DP
type: SiteQuality
SIO_000300: 1.921727e6

VQSLOD
type: SiteQuality
SIO_000300: 9.14e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511532996765319e-5
allele num: 66158
num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: -2.0e-4

FS
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.926e1

DP
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SIO_000300: 1.919752e6

VQSLOD
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SIO_000300: -1.844e0

ClippingRankSum
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QD
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SIO_000300: 1.521e1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66068
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.645061728395061e-5
allele num: 10368
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 count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 3.7e-3

FS
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BaseQRankSum
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SIO_000300: -9.22e-1

VQSLOD
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DP
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ClippingRankSum
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SIO_000300: -2.076e0

MQRankSum
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SIO_000300: -3.84e-1

QD
type: SiteQuality
SIO_000300: 9.109999999999999e0

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 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: 6614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14606
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.516162290011523e-5
allele num: 65956
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

QD
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SIO_000300: 7.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ClippingRankSum
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SIO_000300: -1.041e0

DP
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SIO_000300: 1.904088e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 5.886e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.442e0

GenotypeQuality
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.518741267237713e-5
allele num: 65844
num of homozygotes: 0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.42e-1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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SIO_000300: 4.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-2

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65800
num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 6.981290142418318e-5
allele num: 14324
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: -2.9e-1

FS
type: SiteQuality
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ClippingRankSum
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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African
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VQSLOD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.540784567501772e-5
allele num: 64902
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.716284492809949e-5
allele num: 10292
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Other
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11946
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

MQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 1.155e0

QD
type: SiteQuality
SIO_000300: 1.536e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.864478e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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: 4.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 16

GenotypeQuality
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bin: 9.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14655
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

South Asian
type: Population
allele count: 17
allele frequency: 1.423070483843964e-3
allele num: 11946
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64902
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.536e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

DP
type: SiteQuality
SIO_000300: 1.864478e6

FS
type: SiteQuality
SIO_000300: 1.155e0

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4687
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.083279375944255e-5
allele num: 64866
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11876
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.863708e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

QD
type: SiteQuality
SIO_000300: 1.624e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e0

GenotypeQuality
all individuals: 101
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 219

GenotypeQuality
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GenotypeQuality
all individuals: 40
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variant carriers: 1

GenotypeQuality
all individuals: 2602
bin: 8.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 114
allele frequency: 1.757686021770637e-3
allele num: 64858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 89
allele frequency: 1.345630480798307e-2
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.857198367981348e-4
allele num: 10294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.082725060827251e-4
allele num: 11508
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 4.232266802099204e-4
allele num: 11814
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.207729468599034e-3
allele num: 828
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.375e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.271e1

VQSLOD
type: SiteQuality
SIO_000300: 4.45e0

DP
type: SiteQuality
SIO_000300: 1.872174e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.625489530975362e-5
allele num: 64858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11814
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.271e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.375e0

DP
type: SiteQuality
SIO_000300: 1.872174e6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.926977325477593e-5
allele num: 11202
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
type: SiteQuality
SIO_000300: 1.639e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.128e-1

DP
type: SiteQuality
SIO_000300: 1.862139e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.192e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9904
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.777082518576456e-5
allele num: 10228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64192
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.248e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.627e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.278e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.102e1

DP
type: SiteQuality
SIO_000300: 1.849825e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
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bin: 1.25e1
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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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.115653040877368e-5
allele num: 64192
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.278e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 1.849825e6

QD
type: SiteQuality
SIO_000300: 1.102e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.627e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2290
bin: 7.5e0
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64184
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.166861143523921e-4
allele num: 8570
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.529e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

QD
type: SiteQuality
SIO_000300: 1.239e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.391e0

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

DP
type: SiteQuality
SIO_000300: 1.849625e6

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 499
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GenotypeQuality
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GenotypeQuality
all individuals: 1963
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GenotypeQuality
all individuals: 77
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GenotypeQuality
all individuals: 193
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GenotypeQuality
all individuals: 55
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GenotypeQuality
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bin: 3.75e1
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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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5552
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9876
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64184
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.529e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e0

QD
type: SiteQuality
SIO_000300: 1.239e1

FS
type: SiteQuality
SIO_000300: 3.391e0

VQSLOD
type: SiteQuality
SIO_000300: 3.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

DP
type: SiteQuality
SIO_000300: 1.849625e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.333e0

QD
type: SiteQuality
SIO_000300: 6.66e0

FS
type: SiteQuality
SIO_000300: 5.061e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQRankSum
type: SiteQuality
SIO_000300: -3.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.83e0

DP
type: SiteQuality
SIO_000300: 1.84347e6

VQSLOD
type: SiteQuality
SIO_000300: -1.831e0

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: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.125781445361341e-5
allele num: 63984
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.803921568627451e-5
allele num: 10200
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.13e-1

FS
type: SiteQuality
SIO_000300: 6.411e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 8.61e-1

DP
type: SiteQuality
SIO_000300: 1.843569e6

VQSLOD
type: SiteQuality
SIO_000300: 4.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.12e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9352
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63970
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.74246384387524e-4
allele num: 11478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 1.931e0

DP
type: SiteQuality
SIO_000300: 1.844692e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.025e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 6996
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.072271070126528e-4
allele num: 9326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16078
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

QD
type: SiteQuality
SIO_000300: 5.38e0

FS
type: SiteQuality
SIO_000300: 6.839e0

VQSLOD
type: SiteQuality
SIO_000300: -1.92e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.258e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.303e0

MQ
type: SiteQuality
SIO_000300: 5.718e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 1.743485e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16018
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.719916288803627e-5
allele num: 11468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 9.46e-1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -1.524e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e-1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.632e0

DP
type: SiteQuality
SIO_000300: 1.745232e6

MQ
type: SiteQuality
SIO_000300: 5.805e1

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
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.157063930544593e-5
allele num: 63350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9346
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5700
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

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.949e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.05e0

DP
type: SiteQuality
SIO_000300: 1.731521e6

FS
type: SiteQuality
SIO_000300: 6.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.62e-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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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5700
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9346
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.314127861089187e-5
allele num: 63350
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 808
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-1

FS
type: SiteQuality
SIO_000300: 6.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.731521e6

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

QD
type: SiteQuality
SIO_000300: 1.322e1

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.62e-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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 888
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.177856301531213e-4
allele num: 8490
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65606
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16236
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.063e1

ReadPosRankSum
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SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 5.2e0

DP
type: SiteQuality
SIO_000300: 1.631633e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.78e0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.125949522175937e-5
allele num: 16324
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65808
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-1

FS
type: SiteQuality
SIO_000300: 4.3e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 1.279e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.642263e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.31e0

VQSLOD
type: SiteQuality
SIO_000300: 8.58e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.515151515151515e-4
allele num: 6600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.544215214032537e-5
allele num: 66018
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.37e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 4.602e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 1.649231e6

MQRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.155e0

QD
type: SiteQuality
SIO_000300: 1.366e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.098304671301378e-5
allele num: 16398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66172
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: -2.914e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 6.79e-1

DP
type: SiteQuality
SIO_000300: 1.654112e6

VQSLOD
type: SiteQuality
SIO_000300: -2.415e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.65e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66218
num of homozygotes: 0

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

Latino
type: Population
allele count: 4
allele frequency: 3.466204506065858e-4
allele num: 11540
num of homozygotes: 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: 16412
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 3.475e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.268e1

VQSLOD
type: SiteQuality
SIO_000300: 9.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.655423e6

MQRankSum
type: SiteQuality
SIO_000300: 7.07e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.025003765627353e-5
allele num: 66390
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.661607e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.285e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.853e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1948
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.426301103967002e-4
allele num: 16486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66440
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.98e-1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.662373e6

QD
type: SiteQuality
SIO_000300: 1.274e1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.72e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

GenotypeQuality
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bin: 1.25e1
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
all individuals: 272
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.645061728395061e-5
allele num: 10368
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e-1

DP
type: SiteQuality
SIO_000300: 1.664319e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.85e0

FS
type: SiteQuality
SIO_000300: 5.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.423e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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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bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.645061728395061e-5
allele num: 10368
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66524
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.664319e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e-1

FS
type: SiteQuality
SIO_000300: 5.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.45e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 17
bin: 4.75e1
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GenotypeQuality
all individuals: 274
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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
all individuals: 1963
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502855425308085e-5
allele num: 66540
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.584e0

BaseQRankSum
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SIO_000300: 2.03e0

QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.0471e1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.365e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502810255177181e-5
allele num: 66542
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.926411096127914e-4
allele num: 10382
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: -6.63e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.14e0

QD
type: SiteQuality
SIO_000300: 1.58e1

DP
type: SiteQuality
SIO_000300: 1.664927e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 272
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50253929140247e-5
allele num: 66554
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.181e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

MQRankSum
type: SiteQuality
SIO_000300: -1.275e0

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 1.664767e6

FS
type: SiteQuality
SIO_000300: 4.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
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variant carriers: 0

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

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

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

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

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

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

African
type: Population
allele count: 4
allele frequency: 3.849855630413859e-4
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 1.227e0

DP
type: SiteQuality
SIO_000300: 1.666073e6

QD
type: SiteQuality
SIO_000300: 1.337e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.036e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.46e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 45664
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.885725278953444e-4
allele num: 10396
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
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

European (Non-Finnish)
type: Population
allele count: 73
allele frequency: 1.095898636882243e-3
allele num: 66612
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.845548152634767e-4
allele num: 16510
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

QD
type: SiteQuality
SIO_000300: 1.365e1

VQSLOD
type: SiteQuality
SIO_000300: 4.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.69e-1

DP
type: SiteQuality
SIO_000300: 1.674126e6

FS
type: SiteQuality
SIO_000300: 1.142e0

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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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
all individuals: 2138
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00147072065312e-5
allele num: 66634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 4.29e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

FS
type: SiteQuality
SIO_000300: 1.144e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

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

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

East Asian
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allele count: 0
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allele num: 8644
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
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InbreedingCoeff
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ReadPosRankSum
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QD
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.958e1

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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East Asian
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allele count: 2
allele frequency: 2.313743637204998e-4
allele num: 8644
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66660
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Other
type: Population
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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FS
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
type: SiteQuality
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QD
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DP
type: SiteQuality
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.923076923076923e-4
allele num: 10400
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Other
type: Population
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.043e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.197e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.02e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 7.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.728e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 1.662949e6