15-42136789-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136789
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136789
    reference: chr 15
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1693G>A
  hgvsp: ENSP00000342785.4:p.Ala565Thr
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5577G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1000G>A
  hgvsp: ENSP00000416610.1:p.Ala334Thr
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1304G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1693G>A
  hgvsp: ENSP00000371886.4:p.Ala565Thr
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1693G>A
  hgvsp: ENSP00000441905.2:p.Ala565Thr
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1000G>A
  hgvsp: ENSP00000396045.1:p.Ala334Thr
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5126G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1409G>A
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3898
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4396
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala565Thr
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

15-42136792-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136792
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136792
    reference: chr 15
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5580T>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1003T>G
  hgvsp: ENSP00000396045.1:p.Ser335Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1003T>G
  hgvsp: ENSP00000416610.1:p.Ser335Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1307T>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1412T>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1696T>G
  hgvsp: ENSP00000441905.2:p.Ser566Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1696T>G
  hgvsp: ENSP00000342785.4:p.Ser566Ala
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5129T>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1696T>G
  hgvsp: ENSP00000371886.4:p.Ser566Ala
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7743
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2371
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser566Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

15-42136799-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136799
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136799
    reference: chr 15
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1010C>T
  hgvsp: ENSP00000396045.1:p.Ser337Phe
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1419C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5587C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1703C>T
  hgvsp: ENSP00000441905.2:p.Ser568Phe
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1703C>T
  hgvsp: ENSP00000342785.4:p.Ser568Phe
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1010C>T
  hgvsp: ENSP00000416610.1:p.Ser337Phe
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1703C>T
  hgvsp: ENSP00000371886.4:p.Ser568Phe
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5136C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1314C>T
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser568Phe
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

15-42136806-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136806
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136806
    reference: chr 15
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1709+1G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1016+1G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5142+1G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1709+1G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1709+1G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1425+1G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1320+1G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5593+1G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1016+1G>A
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5592
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1709+1G>A
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

15-42136806-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136806
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136806
    reference: chr 15
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5593+1G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5142+1G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1709+1G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1016+1G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1709+1G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1709+1G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1320+1G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1016+1G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1425+1G>T
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2857
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25384
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
hgvs: c.1709+1G>T
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

15-42136817-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136817
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136817
    reference: chr 15
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1320+12G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5142+12G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1425+12G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1709+12G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1709+12G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1709+12G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1016+12G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5593+12G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1016+12G>A
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2821
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10610
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4354
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3883
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

15-42136817-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136817
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136817
    reference: chr 15
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1016+12G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1709+12G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1425+12G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5142+12G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1320+12G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5593+12G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1709+12G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1016+12G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1709+12G>T
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4354
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3883
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

15-42136822-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136822
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136822
    reference: chr 15
allele count: 1
allele frequency: 8.27034090345204e-6
allele num: 120914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5142+17C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1320+17C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1016+17C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1709+17C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1709+17C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1425+17C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1016+17C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1709+17C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5593+17C>T
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8859
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7719
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25373
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum

15-42136843-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136843
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136841
    reference: chr 15
allele count: 2
allele frequency: 1.659888787451241e-5
allele num: 120490
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1709+39_1709+40delAG
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5142+39_5142+40delAG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1016+39_1016+40delAG
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1320+39_*1320+40delAG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1709+39_1709+40delAG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5593+39_5593+40delAG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1709+39_1709+40delAG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1016+39_1016+40delAG
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1425+39_1425+40delAG
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7670
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: CAG
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/15-42136844-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136844
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136844
    reference: chr 15
allele count: 2
allele frequency: 1.66008167601846e-5
allele num: 120476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1709+39A>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1016+39A>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5593+39A>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1709+39A>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1016+39A>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5142+39A>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1320+39A>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1709+39A>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1425+39A>C
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4696
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

15-42136844-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136844
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136843
    reference: chr 15
allele count: 1
allele frequency: 8.300408380092301e-6
allele num: 120476
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1016+44delG
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1709+44delG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1016+44delG
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5593+44delG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1709+44delG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1709+44delG
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1425+44delG
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1320+44delG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5142+44delG
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8639
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8236
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2339
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8343
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: AG
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

15-42136848-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136848
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136848
    reference: chr 15
allele count: 2
allele frequency: 1.662703889064397e-5
allele num: 120286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5142+43G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1425+43G>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5593+43G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1709+43G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1709+43G>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1320+43G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1709+43G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1016+43G>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1016+43G>C
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2601
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

15-42136849-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136849
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136849
    reference: chr 15
allele count: 1
allele frequency: 8.311446524153063e-6
allele num: 120316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5142+44G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1016+44G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1320+44G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1709+44G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1016+44G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1709+44G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5593+44G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1425+44G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1709+44G>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3065
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8545
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7584
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2330
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3857
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

15-42136854-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136854
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136854
    reference: chr 15
allele count: 1
allele frequency: 8.329585020074299e-6
allele num: 120054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1016+49G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1016+49G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5142+49G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1425+49G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1320+49G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1709+49G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1709+49G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5593+49G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1709+49G>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4348
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25313
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5320
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

15-42136997-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136997
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136997
    reference: chr 15
allele count: 1
allele frequency: 2.532286654849329e-5
allele num: 39490
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-49C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-49C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-49C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-49C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-49C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-49C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-49C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-49C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-49C>T
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13122
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26501
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12002
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11648
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

15-42136998-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42136998
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42136998
    reference: chr 15
allele count: 1
allele frequency: 2.525252525252525e-5
allele num: 39600
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-48G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-48G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-48G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-48G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-48G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-48G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-48G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-48G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-48G>A
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13075
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12021
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26519
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1816
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11914
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/15-42137003-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137003
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137003
    reference: chr 15
allele count: 1
allele frequency: 2.488800398208064e-5
allele num: 40180
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-43C>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-43C>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-43C>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-43C>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-43C>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-43C>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-43C>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-43C>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-43C>A
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12840
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12072
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4690
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12493
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4386
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22104
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3595
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

15-42137017-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137017
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137017
    reference: chr 15
allele count: 1
allele frequency: 2.418730650154799e-5
allele num: 41344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-29C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-29C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-29C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-29C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-29C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-29C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-29C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-29C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-29C>T
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12688
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24445
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3455
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3252
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

15-42137020-C-CTGGCTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137020
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137026
    reference: chr 15
allele count: 10
allele frequency: 2.43107891282151e-4
allele num: 41134
alternate allele: CTGGCTT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-12_1426-7dupGGCTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-12_1710-7dupGGCTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-12_*1321-7dupGGCTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-12_5594-7dupGGCTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-12_1017-7dupGGCTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-12_1710-7dupGGCTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-12_5143-7dupGGCTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-12_1017-7dupGGCTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-12_1710-7dupGGCTTT
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26987
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12787
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13005
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3526
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

15-42137020-CTGGCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137020
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137014
    reference: chr 15
allele count: 63
allele frequency: 1.531579715077551e-3
allele num: 41134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-12_1710-7delGGCTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-12_1017-7delGGCTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-12_1426-7delGGCTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-12_1017-7delGGCTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-12_*1321-7delGGCTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-12_5143-7delGGCTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-12_1710-7delGGCTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-12_1710-7delGGCTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-12_5594-7delGGCTTT
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12787
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 9518
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4141
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26987
  bin: 7.5e0
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3333
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1393
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23671
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2942
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: CTGGCTT
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

15-42137023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137023
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137023
    reference: chr 15
allele count: 1
allele frequency: 2.514331690636629e-5
allele num: 39772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-23G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-23G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-23G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-23G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-23G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-23G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-23G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-23G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-23G>A
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3519
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4205
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum

15-42137024-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137024
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137024
    reference: chr 15
allele count: 1
allele frequency: 2.490411914130597e-5
allele num: 40154
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-22C>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-22C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-22C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-22C>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-22C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-22C>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-22C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-22C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-22C>G
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12969
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3291
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4457
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3351
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-42137028-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137028
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137028
    reference: chr 15
allele count: 1
allele frequency: 2.37925291458482e-5
allele num: 42030
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-18G>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-18G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-18G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-18G>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-18G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-18G>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-18G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-18G>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-18G>C
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7467
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12765
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24235
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

15-42137030-CTTTGGCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137030
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137023
    reference: chr 15
allele count: 1
allele frequency: 2.334267040149393e-5
allele num: 42840
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-12_1017-6delGGCTTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-12_1710-6delGGCTTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-12_1017-6delGGCTTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-12_5143-6delGGCTTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-12_*1321-6delGGCTTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-12_1710-6delGGCTTTT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-12_1710-6delGGCTTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-12_1426-6delGGCTTTT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-12_5594-6delGGCTTTT
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6983
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26096
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3094
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9965
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3241
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: CTTTGGCT
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

15-42137034-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137034
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137034
    reference: chr 15
allele count: 1
allele frequency: 2.276037873270211e-5
allele num: 43936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-12G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-12G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-12G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-12G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-12G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-12G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-12G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-12G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-12G>T
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12218
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25165
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

15-42137035-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137035
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137035
    reference: chr 15
allele count: 1
allele frequency: 2.257642118571364e-5
allele num: 44294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-11G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-11G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-11G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-11G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-11G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-11G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-11G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-11G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-11G>A
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25926
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2934
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2456
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

15-42137036-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137036
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137035
    reference: chr 15
allele count: 15268
allele frequency: 2.578183046268153e-1
allele num: 59220
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710-6delT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321-6delT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017-6delT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017-6delT
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143-6delT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594-6delT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710-6delT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710-6delT
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426-6delT
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 2.75e1
  variant carriers: 851
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 1.75e1
  variant carriers: 3417
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 174
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 2.5e0
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 3.25e1
  variant carriers: 488
genotype depth: GenotypeDepth
  all individuals: 13416
  bin: 1.25e1
  variant carriers: 5862
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 315
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 6.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 25206
  bin: 7.5e0
  variant carriers: 3751
genotype depth: GenotypeDepth
  all individuals: 7447
  bin: 2.25e1
  variant carriers: 1648
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 40
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 3.25e1
  variant carriers: 457
genotype quality: GenotypeQuality
  all individuals: 1457
  bin: 1.75e1
  variant carriers: 453
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 8.75e1
  variant carriers: 133
genotype quality: GenotypeQuality
  all individuals: 4011
  bin: 7.5e0
  variant carriers: 163
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 323
genotype quality: GenotypeQuality
  all individuals: 6793
  bin: 6.25e1
  variant carriers: 309
num of homozygotes: 2201
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: CT
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

15-42137046-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137046
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137046
    reference: chr 15
allele count: 1
allele frequency: 1.555984315678098e-5
allele num: 64268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1426G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1017G>A
  hgvsp: ENSP00000416610.1:p.Trp339Ter
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5594G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1710G>A
  hgvsp: ENSP00000342785.4:p.Trp570Ter
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1710G>A
  hgvsp: ENSP00000441905.2:p.Trp570Ter
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1710G>A
  hgvsp: ENSP00000371886.4:p.Trp570Ter
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1017G>A
  hgvsp: ENSP00000396045.1:p.Trp339Ter
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5143G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1321G>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Trp570Ter
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

15-42137054-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137054
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137054
    reference: chr 15
allele count: 2
allele frequency: 2.928772258669166e-5
allele num: 68288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1718C>T
  hgvsp: ENSP00000342785.4:p.Ala573Val
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1718C>T
  hgvsp: ENSP00000441905.2:p.Ala573Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5602C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1718C>T
  hgvsp: ENSP00000371886.4:p.Ala573Val
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5151C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1329C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1025C>T
  hgvsp: ENSP00000416610.1:p.Ala342Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1025C>T
  hgvsp: ENSP00000396045.1:p.Ala342Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1434C>T
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12656
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2190
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala573Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/15-42137058-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137058
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137058
    reference: chr 15
allele count: 2
allele frequency: 2.813493514897448e-5
allele num: 71086
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1722C>A
  hgvsp: ENSP00000441905.2:p.Asn574Lys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1722C>A
  hgvsp: ENSP00000371886.4:p.Asn574Lys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1438C>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1333C>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1029C>A
  hgvsp: ENSP00000416610.1:p.Asn343Lys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1722C>A
  hgvsp: ENSP00000342785.4:p.Asn574Lys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5155C>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5606C>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1029C>A
  hgvsp: ENSP00000396045.1:p.Asn343Lys
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11314
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23130
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14823
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3959
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1837
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn574Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

15-42137063-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137063
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137063
    reference: chr 15
allele count: 3
allele frequency: 4.064269650743762e-5
allele num: 73814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5611A>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1443A>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5160A>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1727A>G
  hgvsp: ENSP00000342785.4:p.Tyr576Cys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1034A>G
  hgvsp: ENSP00000416610.1:p.Tyr345Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1338A>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1727A>G
  hgvsp: ENSP00000441905.2:p.Tyr576Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1034A>G
  hgvsp: ENSP00000396045.1:p.Tyr345Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1727A>G
  hgvsp: ENSP00000371886.4:p.Tyr576Cys
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4893
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10391
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23638
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr576Cys
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-42137067-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137067
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137067
    reference: chr 15
allele count: 1
allele frequency: 1.314025912590996e-5
allele num: 76102
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1038G>A
  hgvsp: ENST00000458483.1:c.1038G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1038G>A
  hgvsp: ENST00000452633.1:c.1038G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1731G>A
  hgvsp: ENST00000382448.4:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5615G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1731G>A
  hgvsp: ENST00000342159.4:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1731G>A
  hgvsp: ENST00000542534.2:c.1731G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1447G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1342G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5164G>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18960
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9695
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu577Glu
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-42137071-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137071
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137071
    reference: chr 15
allele count: 1
allele frequency: 1.274599775670439e-5
allele num: 78456
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1451C>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1735C>G
  hgvsp: ENSP00000342785.4:p.Pro579Ala
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1346C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1735C>G
  hgvsp: ENSP00000441905.2:p.Pro579Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1735C>G
  hgvsp: ENSP00000371886.4:p.Pro579Ala
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1042C>G
  hgvsp: ENSP00000396045.1:p.Pro348Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5619C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1042C>G
  hgvsp: ENSP00000416610.1:p.Pro348Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5168C>G
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9044
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3011
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro579Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

15-42137074-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137074
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137074
    reference: chr 15
allele count: 1
allele frequency: 1.238420765839402e-5
allele num: 80748
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1738G>A
  hgvsp: ENSP00000441905.2:p.Glu580Lys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1045G>A
  hgvsp: ENSP00000396045.1:p.Glu349Lys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1045G>A
  hgvsp: ENSP00000416610.1:p.Glu349Lys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5171G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1349G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1738G>A
  hgvsp: ENSP00000342785.4:p.Glu580Lys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1738G>A
  hgvsp: ENSP00000371886.4:p.Glu580Lys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1454G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5622G>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22301
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24742
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2153
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu580Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

15-42137077-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137077
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137077
    reference: chr 15
allele count: 1
allele frequency: 1.216071602295943e-5
allele num: 82232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1741T>C
  hgvsp: ENSP00000342785.4:p.Trp581Arg
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1741T>C
  hgvsp: ENSP00000441905.2:p.Trp581Arg
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1741T>C
  hgvsp: ENSP00000371886.4:p.Trp581Arg
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1352T>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5625T>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1048T>C
  hgvsp: ENSP00000416610.1:p.Trp350Arg
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1457T>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5174T>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1048T>C
  hgvsp: ENSP00000396045.1:p.Trp350Arg
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2512
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1425
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Trp581Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

15-42137079-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137079
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137079
    reference: chr 15
allele count: 1
allele frequency: 1.201258919347476e-5
allele num: 83246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1354G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5627G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1050G>A
  hgvsp: ENSP00000396045.1:p.Trp350Ter
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1743G>A
  hgvsp: ENSP00000371886.4:p.Trp581Ter
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5176G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1050G>A
  hgvsp: ENSP00000416610.1:p.Trp350Ter
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1743G>A
  hgvsp: ENSP00000342785.4:p.Trp581Ter
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1459G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1743G>A
  hgvsp: ENSP00000441905.2:p.Trp581Ter
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7788
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2261
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Trp581Ter
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

15-42137080-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137080
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137080
    reference: chr 15
allele count: 1
allele frequency: 1.195228647240217e-5
allele num: 83666
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1744T>C
  hgvsp: ENSP00000441905.2:p.Ser582Pro
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1744T>C
  hgvsp: ENSP00000371886.4:p.Ser582Pro
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5177T>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1744T>C
  hgvsp: ENSP00000342785.4:p.Ser582Pro
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1355T>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1460T>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1051T>C
  hgvsp: ENSP00000416610.1:p.Ser351Pro
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1051T>C
  hgvsp: ENSP00000396045.1:p.Ser351Pro
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5628T>C
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7688
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23991
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17989
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2459
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19896
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser582Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD

15-42137085-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137085
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137085
    reference: chr 15
allele count: 1
allele frequency: 1.164958061509786e-5
allele num: 85840
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1749G>A
  hgvsp: ENST00000382448.4:c.1749G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1749G>A
  hgvsp: ENST00000342159.4:c.1749G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1056G>A
  hgvsp: ENST00000452633.1:c.1056G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1360G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1749G>A
  hgvsp: ENST00000542534.2:c.1749G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1465G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1056G>A
  hgvsp: ENST00000458483.1:c.1056G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5633G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5182G>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25288
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln583Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-42137092-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137092
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137092
    reference: chr 15
allele count: 1
allele frequency: 1.138200277720868e-5
allele num: 87858
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1756C>G
  hgvsp: ENSP00000342785.4:p.Leu586Val
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1367C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5640C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5189C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1063C>G
  hgvsp: ENSP00000416610.1:p.Leu355Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1063C>G
  hgvsp: ENSP00000396045.1:p.Leu355Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1472C>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1756C>G
  hgvsp: ENSP00000441905.2:p.Leu586Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1756C>G
  hgvsp: ENSP00000371886.4:p.Leu586Val
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6565
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6843
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15998
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18077
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu586Val
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

15-42137096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137096
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137096
    reference: chr 15
allele count: 1
allele frequency: 1.118868600071608e-5
allele num: 89376
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1760C>T
  hgvsp: ENSP00000371886.4:p.Ala587Val
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1371C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1476C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1760C>T
  hgvsp: ENSP00000342785.4:p.Ala587Val
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1067C>T
  hgvsp: ENSP00000396045.1:p.Ala356Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5644C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1760C>T
  hgvsp: ENSP00000441905.2:p.Ala587Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1067C>T
  hgvsp: ENSP00000416610.1:p.Ala356Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5193C>T
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1878
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29673
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala587Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

15-42137104-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137104
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137104
    reference: chr 15
allele count: 14
allele frequency: 1.526051885764116e-4
allele num: 91740
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1768A>G
  hgvsp: ENSP00000342785.4:p.Thr590Ala
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5652A>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1484A>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1768A>G
  hgvsp: ENSP00000441905.2:p.Thr590Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1768A>G
  hgvsp: ENSP00000371886.4:p.Thr590Ala
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1379A>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1075A>G
  hgvsp: ENSP00000416610.1:p.Thr359Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1075A>G
  hgvsp: ENSP00000396045.1:p.Thr359Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5201A>G
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7222
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27717
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6366
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr590Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/15-42137108-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137108
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137108
    reference: chr 15
allele count: 4
allele frequency: 4.327880204275946e-5
allele num: 92424
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1488A>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5656A>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1772A>C
  hgvsp: ENSP00000371886.4:p.Glu591Ala
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1383A>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1079A>C
  hgvsp: ENSP00000416610.1:p.Glu360Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1772A>C
  hgvsp: ENSP00000342785.4:p.Glu591Ala
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1772A>C
  hgvsp: ENSP00000441905.2:p.Glu591Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1079A>C
  hgvsp: ENSP00000396045.1:p.Glu360Ala
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5205A>C
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27786
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu591Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

15-42137120-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137120
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137120
    reference: chr 15
allele count: 1
allele frequency: 1.066712179719668e-5
allele num: 93746
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1784C>T
  hgvsp: ENSP00000371886.4:p.Thr595Ile
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1091C>T
  hgvsp: ENSP00000396045.1:p.Thr364Ile
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1784C>T
  hgvsp: ENSP00000342785.4:p.Thr595Ile
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1395C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1784C>T
  hgvsp: ENSP00000441905.2:p.Thr595Ile
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5217C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1091C>T
  hgvsp: ENSP00000416610.1:p.Thr364Ile
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1500C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5668C>T
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr595Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-42137136-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137136
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137135
    reference: chr 15
allele count: 1
allele frequency: 1.067440917145236e-5
allele num: 93682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5686delA
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1802delA
  hgvsp: ENSP00000371886.4:p.Lys601SerfsTer57
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1109delA
  hgvsp: ENSP00000396045.1:p.Lys370SerfsTer57
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1518delA
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5235delA
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1109delA
  hgvsp: ENSP00000416610.1:p.Lys370SerfsTer57
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1802delA
  hgvsp: ENSP00000342785.4:p.Lys601SerfsTer57
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1802delA
  hgvsp: ENSP00000441905.2:p.Lys601SerfsTer57
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1413delA
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2523
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys601SerfsTer57
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: CA
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ

15-42137137-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137137
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137137
    reference: chr 15
allele count: 1
allele frequency: 1.068239114643422e-5
allele num: 93612
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1108A>G
  hgvsp: ENSP00000396045.1:p.Lys370Glu
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5234A>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1801A>G
  hgvsp: ENSP00000371886.4:p.Lys601Glu
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1412A>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1801A>G
  hgvsp: ENSP00000342785.4:p.Lys601Glu
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1108A>G
  hgvsp: ENSP00000416610.1:p.Lys370Glu
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5685A>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1517A>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1801A>G
  hgvsp: ENSP00000441905.2:p.Lys601Glu
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27550
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys601Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

15-42137139-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137139
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137139
    reference: chr 15
allele count: 1
allele frequency: 1.081361650590423e-5
allele num: 92476
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1803G>A
  hgvsp: ENST00000542534.2:c.1803G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1803G>A
  hgvsp: ENST00000342159.4:c.1803G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1803G>A
  hgvsp: ENST00000382448.4:c.1803G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5236G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1110G>A
  hgvsp: ENST00000458483.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1414G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1110G>A
  hgvsp: ENST00000452633.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1519G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5687G>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10018
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2808
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys601Lys
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

15-42137149-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137149
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137149
    reference: chr 15
allele count: 9
allele frequency: 9.796238244514106e-5
allele num: 91872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1120C>G
  hgvsp: ENSP00000396045.1:p.Leu374Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1813C>G
  hgvsp: ENSP00000371886.4:p.Leu605Val
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1120C>G
  hgvsp: ENSP00000416610.1:p.Leu374Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1529C>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1424C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5697C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1813C>G
  hgvsp: ENSP00000441905.2:p.Leu605Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5246C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1813C>G
  hgvsp: ENSP00000342785.4:p.Leu605Val
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20826
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11183
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7147
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3057
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu605Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-42137152-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137152
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137152
    reference: chr 15
allele count: 32
allele frequency: 3.500940877860925e-4
allele num: 91404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1123G>T
  hgvsp: ENSP00000396045.1:p.Ala375Ser
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5700G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1532G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1816G>T
  hgvsp: ENSP00000441905.2:p.Ala606Ser
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1427G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1816G>T
  hgvsp: ENSP00000342785.4:p.Ala606Ser
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5249G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1123G>T
  hgvsp: ENSP00000416610.1:p.Ala375Ser
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1816G>T
  hgvsp: ENSP00000371886.4:p.Ala606Ser
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11729
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7088
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13796
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20079
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22404
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1337
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1857
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala606Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-42137155-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137155
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137155
    reference: chr 15
allele count: 2
allele frequency: 2.185362442361066e-5
allele num: 91518
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1819C>A
  hgvsp: ENSP00000371886.4:p.Pro607Thr
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1126C>A
  hgvsp: ENSP00000396045.1:p.Pro376Thr
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1126C>A
  hgvsp: ENSP00000416610.1:p.Pro376Thr
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1819C>A
  hgvsp: ENSP00000342785.4:p.Pro607Thr
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1819C>A
  hgvsp: ENSP00000441905.2:p.Pro607Thr
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1535C>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5252C>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1430C>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5703C>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19550
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2277
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro607Thr
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

15-42137155-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137155
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137155
    reference: chr 15
allele count: 1
allele frequency: 1.092681221180533e-5
allele num: 91518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1126C>T
  hgvsp: ENSP00000396045.1:p.Pro376Ser
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1430C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1819C>T
  hgvsp: ENSP00000371886.4:p.Pro607Ser
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1819C>T
  hgvsp: ENSP00000342785.4:p.Pro607Ser
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1126C>T
  hgvsp: ENSP00000416610.1:p.Pro376Ser
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1535C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5703C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5252C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1819C>T
  hgvsp: ENSP00000441905.2:p.Pro607Ser
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19550
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1830
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro607Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum

15-42137161-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137161
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137161
    reference: chr 15
allele count: 29
allele frequency: 3.203287235452658e-4
allele num: 90532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1132C>T
  hgvsp: ENSP00000416610.1:p.Gln378Ter
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1436C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1825C>T
  hgvsp: ENSP00000441905.2:p.Gln609Ter
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1132C>T
  hgvsp: ENSP00000396045.1:p.Gln378Ter
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5709C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1825C>T
  hgvsp: ENSP00000342785.4:p.Gln609Ter
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5258C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1541C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1825C>T
  hgvsp: ENSP00000371886.4:p.Gln609Ter
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18485
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7062
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13100
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14271
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln609Ter
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

15-42137163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137163
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137163
    reference: chr 15
allele count: 1
allele frequency: 1.109557730288707e-5
allele num: 90126
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1134G>A
  hgvsp: ENST00000458483.1:c.1134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5711G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1543G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5260G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1438G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1827G>A
  hgvsp: ENST00000542534.2:c.1827G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1827G>A
  hgvsp: ENST00000342159.4:c.1827G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1134G>A
  hgvsp: ENST00000452633.1:c.1134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1827G>A
  hgvsp: ENST00000382448.4:c.1827G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4894
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18059
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21663
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1988
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln609Gln
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

15-42137164-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137164
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137164
    reference: chr 15
allele count: 1
allele frequency: 1.111481604979438e-5
allele num: 89970
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5712C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1828C>G
  hgvsp: ENSP00000342785.4:p.Leu610Val
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1828C>G
  hgvsp: ENSP00000441905.2:p.Leu610Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1544C>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1135C>G
  hgvsp: ENSP00000416610.1:p.Leu379Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1439C>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1135C>G
  hgvsp: ENSP00000396045.1:p.Leu379Val
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1828C>G
  hgvsp: ENSP00000371886.4:p.Leu610Val
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5261C>G
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21224
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu610Val
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD

15-42137170-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137170
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137170
    reference: chr 15
allele count: 11
allele frequency: 1.247363527090468e-4
allele num: 88186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5267C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1141C>T
  hgvsp: ENSP00000396045.1:p.Arg381Trp
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1445C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1834C>T
  hgvsp: ENSP00000371886.4:p.Arg612Trp
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5718C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1141C>T
  hgvsp: ENSP00000416610.1:p.Arg381Trp
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1550C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1834C>T
  hgvsp: ENSP00000342785.4:p.Arg612Trp
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1834C>T
  hgvsp: ENSP00000441905.2:p.Arg612Trp
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15022
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14883
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6595
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15808
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg612Trp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

15-42137171-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137171
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137171
    reference: chr 15
allele count: 3
allele frequency: 3.440366972477065e-5
allele num: 87200
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1835G>A
  hgvsp: ENSP00000441905.2:p.Arg612Gln
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5268G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1835G>A
  hgvsp: ENSP00000371886.4:p.Arg612Gln
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1446G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1835G>A
  hgvsp: ENSP00000342785.4:p.Arg612Gln
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1551G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1142G>A
  hgvsp: ENSP00000396045.1:p.Arg381Gln
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1142G>A
  hgvsp: ENSP00000416610.1:p.Arg381Gln
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5719G>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15145
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5578
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14749
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15675
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22790
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16495
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg612Gln
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ

15-42137176-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137176
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137176
    reference: chr 15
allele count: 9
allele frequency: 1.038781163434903e-4
allele num: 86640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5273C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1840C>T
  hgvsp: ENSP00000371886.4:p.Arg614Trp
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5724C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1147C>T
  hgvsp: ENSP00000396045.1:p.Arg383Trp
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1556C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1840C>T
  hgvsp: ENSP00000441905.2:p.Arg614Trp
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1147C>T
  hgvsp: ENSP00000416610.1:p.Arg383Trp
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1840C>T
  hgvsp: ENSP00000342785.4:p.Arg614Trp
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1451C>T
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14155
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16238
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6242
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15359
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4176
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23464
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg614Trp
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

15-42137177-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137177
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137177
    reference: chr 15
allele count: 3
allele frequency: 3.515103226864762e-5
allele num: 85346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5274G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1841G>A
  hgvsp: ENSP00000371886.4:p.Arg614Gln
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1841G>A
  hgvsp: ENSP00000441905.2:p.Arg614Gln
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1452G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1557G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1148G>A
  hgvsp: ENSP00000416610.1:p.Arg383Gln
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1841G>A
  hgvsp: ENSP00000342785.4:p.Arg614Gln
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1148G>A
  hgvsp: ENSP00000396045.1:p.Arg383Gln
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5725G>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15732
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12893
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4481
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1917
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23635
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg614Gln
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

15-42137180-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137180
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137180
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 85808
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5277A>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5728A>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1844A>G
  hgvsp: ENSP00000342785.4:p.Gln615Arg
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1844A>G
  hgvsp: ENSP00000441905.2:p.Gln615Arg
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1560A>G
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1151A>G
  hgvsp: ENSP00000416610.1:p.Gln384Arg
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1455A>G
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1151A>G
  hgvsp: ENSP00000396045.1:p.Gln384Arg
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1844A>G
  hgvsp: ENSP00000371886.4:p.Gln615Arg
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13011
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln615Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

15-42137188-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137188
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137188
    reference: chr 15
allele count: 1
allele frequency: 1.217848791893998e-5
allele num: 82112
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1852G>A
  hgvsp: ENSP00000441905.2:p.Ala618Thr
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1159G>A
  hgvsp: ENSP00000396045.1:p.Ala387Thr
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1852G>A
  hgvsp: ENSP00000342785.4:p.Ala618Thr
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1159G>A
  hgvsp: ENSP00000416610.1:p.Ala387Thr
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5736G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5285G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1852G>A
  hgvsp: ENSP00000371886.4:p.Ala618Thr
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1568G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1463G>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24611
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4832
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala618Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

15-42137190-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137190
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137190
    reference: chr 15
allele count: 5
allele frequency: 6.20670821023362e-5
allele num: 80558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1161C>T
  hgvsp: ENST00000452633.1:c.1161C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1465C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1854C>T
  hgvsp: ENST00000342159.4:c.1854C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1161C>T
  hgvsp: ENST00000458483.1:c.1161C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1854C>T
  hgvsp: ENST00000542534.2:c.1854C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1570C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1854C>T
  hgvsp: ENST00000382448.4:c.1854C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5287C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5738C>T
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18039
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17418
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10605
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24199
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala618Ala
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

15-42137191-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137191
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137191
    reference: chr 15
allele count: 1
allele frequency: 1.240233163834801e-5
allele num: 80630
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5739G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5288G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1855G>A
  hgvsp: ENSP00000342785.4:p.Glu619Lys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1571G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1162G>A
  hgvsp: ENSP00000416610.1:p.Glu388Lys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1466G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1855G>A
  hgvsp: ENSP00000441905.2:p.Glu619Lys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1855G>A
  hgvsp: ENSP00000371886.4:p.Glu619Lys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1162G>A
  hgvsp: ENSP00000396045.1:p.Glu388Lys
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10698
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4825
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5008
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu619Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ

15-42137194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137194
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137194
    reference: chr 15
allele count: 1
allele frequency: 1.246882793017456e-5
allele num: 80200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5291C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1858C>T
  hgvsp: ENSP00000371886.4:p.Arg620Cys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5742C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1858C>T
  hgvsp: ENSP00000342785.4:p.Arg620Cys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1165C>T
  hgvsp: ENSP00000416610.1:p.Arg389Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1858C>T
  hgvsp: ENSP00000441905.2:p.Arg620Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1165C>T
  hgvsp: ENSP00000396045.1:p.Arg389Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1574C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1469C>T
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4348
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg620Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

15-42137195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137195
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137195
    reference: chr 15
allele count: 1
allele frequency: 1.25281884239539e-5
allele num: 79820
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1859G>A
  hgvsp: ENSP00000342785.4:p.Arg620His
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5292G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5743G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1470G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1166G>A
  hgvsp: ENSP00000416610.1:p.Arg389His
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1859G>A
  hgvsp: ENSP00000441905.2:p.Arg620His
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1575G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1859G>A
  hgvsp: ENSP00000371886.4:p.Arg620His
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1166G>A
  hgvsp: ENSP00000396045.1:p.Arg389His
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18202
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5044
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25159
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg620His
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

15-42137200-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137200
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137200
    reference: chr 15
allele count: 22
allele frequency: 2.793934621929847e-4
allele num: 78742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1864C>T
  hgvsp: ENSP00000342785.4:p.Arg622Cys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5297C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1171C>T
  hgvsp: ENSP00000396045.1:p.Arg391Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1580C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5748C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1171C>T
  hgvsp: ENSP00000416610.1:p.Arg391Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1864C>T
  hgvsp: ENSP00000441905.2:p.Arg622Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1475C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1864C>T
  hgvsp: ENSP00000371886.4:p.Arg622Cys
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18249
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18326
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10479
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5045
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg622Cys
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

15-42137201-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137201
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137201
    reference: chr 15
allele count: 420
allele frequency: 5.364532774740714e-3
allele num: 78292
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1865G>A
  hgvsp: ENSP00000441905.2:p.Arg622His
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5298G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1865G>A
  hgvsp: ENSP00000342785.4:p.Arg622His
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1172G>A
  hgvsp: ENSP00000416610.1:p.Arg391His
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1581G>A
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1865G>A
  hgvsp: ENSP00000371886.4:p.Arg622His
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1172G>A
  hgvsp: ENSP00000396045.1:p.Arg391His
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5749G>A
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1476G>A
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 1.75e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 10491
  bin: 2.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18289
  bin: 7.5e0
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 2.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 18385
  bin: 1.25e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 3.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4741
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 25772
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 9.25e1
  variant carriers: 11
hgvs: p.Arg622His
num of homozygotes: 10
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

15-42137204-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137204
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137205
    reference: chr 15
allele count: 1
allele frequency: 1.277465508431272e-5
allele num: 78280
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1178dupG
  hgvsp: ENSP00000396045.1:p.Tyr394LeufsTer19
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5304dupG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5755dupG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1871dupG
  hgvsp: ENSP00000342785.4:p.Tyr625LeufsTer19
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1587dupG
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1178dupG
  hgvsp: ENSP00000416610.1:p.Tyr394LeufsTer19
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1482dupG
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1871dupG
  hgvsp: ENSP00000441905.2:p.Tyr625LeufsTer19
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1871dupG
  hgvsp: ENSP00000371886.4:p.Tyr625LeufsTer19
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4889
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10505
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18637
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12227
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4817
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr625LeufsTer19
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

15-42137206-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137206
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137206
    reference: chr 15
allele count: 1
allele frequency: 1.288792659037014e-5
allele num: 77592
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1870G>T
  hgvsp: ENSP00000441905.2:p.Gly624Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1481G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1586G>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5303G>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1177G>T
  hgvsp: ENSP00000396045.1:p.Gly393Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1870G>T
  hgvsp: ENSP00000371886.4:p.Gly624Cys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1870G>T
  hgvsp: ENSP00000342785.4:p.Gly624Cys
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1177G>T
  hgvsp: ENSP00000416610.1:p.Gly393Cys
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5754G>T
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10033
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11416
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly624Cys
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

15-42137211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137211
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137211
    reference: chr 15
allele count: 1
allele frequency: 1.298532658096351e-5
allele num: 77010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1182C>T
  hgvsp: ENST00000452633.1:c.1182C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1182C>T
  hgvsp: ENST00000458483.1:c.1182C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1875C>T
  hgvsp: ENST00000542534.2:c.1875C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1875C>T
  hgvsp: ENST00000382448.4:c.1875C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5308C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1486C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1591C>T
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5759C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1875C>T
  hgvsp: ENST00000342159.4:c.1875C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3677
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18984
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18986
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2868
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr625Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

15-42137216-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137216
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137216
    reference: chr 15
allele count: 34
allele frequency: 4.440613327064232e-4
allele num: 76566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1880G>C
  hgvsp: ENSP00000342785.4:p.Ser627Thr
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1187G>C
  hgvsp: ENSP00000416610.1:p.Ser396Thr
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1596G>C
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5764G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1880G>C
  hgvsp: ENSP00000441905.2:p.Ser627Thr
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1491G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1880G>C
  hgvsp: ENSP00000371886.4:p.Ser627Thr
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5313G>C
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1187G>C
  hgvsp: ENSP00000396045.1:p.Ser396Thr
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19183
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19175
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 9.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11141
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser627Thr
num of homozygotes: 1
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

15-42137223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 42137223
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 42137223
    reference: chr 15
allele count: 22
allele frequency: 2.915915597497614e-4
allele num: 75448
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000371886
  ensembl transcript: ENST00000382448
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000382448.4:c.1887C>T
  hgvsp: ENST00000382448.4:c.1887C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000490848
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000490848.1:n.5771C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000396045
  ensembl transcript: ENST00000452633
  gene symbol: PLA2G4B
  hgvsc: ENST00000452633.1:c.1194C>T
  hgvsp: ENST00000452633.1:c.1194C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000416610
  ensembl transcript: ENST00000458483
  gene symbol: PLA2G4B
  hgvsc: ENST00000458483.1:c.1194C>T
  hgvsp: ENST00000458483.1:c.1194C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000243708
  ensembl protein: ENSP00000441905
  ensembl transcript: ENST00000542534
  gene symbol: PLA2G4B
  hgvsc: ENST00000542534.2:c.1887C>T
  hgvsp: ENST00000542534.2:c.1887C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9036
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000424127
  ensembl transcript: ENST00000487292
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000487292.1:c.*1498C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000168970
  ensembl transcript: ENST00000491746
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000491746.1:n.5320C>T
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000168970
  ensembl protein: ENSP00000342785
  ensembl transcript: ENST00000342159
  gene symbol: JMJD7-PLA2G4B
  hgvsc: ENST00000342159.4:c.1887C>T
  hgvsp: ENST00000342159.4:c.1887C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/34449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000243708
  ensembl transcript: ENST00000483748
  gene symbol: PLA2G4B
  hgvsc: ENST00000483748.1:n.1603C>T
  variant of: http://identifiers.org/hgnc/9036
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19599
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8467
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe629Phe
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5680
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2371
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4421
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2876
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11324
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25401
bin: 9.75e1
variant carriers: 1

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.212e1

MQRankSum
type: SiteQuality
SIO_000300: -2.177e0

FS
type: SiteQuality
SIO_000300: 4.566e0

VQSLOD
type: SiteQuality
SIO_000300: -1.364e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.28e-1

DP
type: SiteQuality
SIO_000300: 2.471084e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e0

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4418
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5672
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3894
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25399
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2873
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11268
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.052e1

MQRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.618e0

VQSLOD
type: SiteQuality
SIO_000300: 1.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e-1

DP
type: SiteQuality
SIO_000300: 2.46979e6

GenotypeQuality
all individuals: 11159
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3891
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5634
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25387
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 262
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2865
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4395
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4407
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
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: 1
allele frequency: 9.648784253184099e-5
allele num: 10364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 7.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.364e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

DP
type: SiteQuality
SIO_000300: 2.466369e6

QD
type: SiteQuality
SIO_000300: 1.341e1

MQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.75e1
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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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bin: 3.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.535e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 2.462961e6

FS
type: SiteQuality
SIO_000300: 2.122e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.104e1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

East Asian
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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: 10358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 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: 904
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.535e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 1.104e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-1

FS
type: SiteQuality
SIO_000300: 2.122e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.462961e6

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

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.3e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 2.454817e6

FS
type: SiteQuality
SIO_000300: 1.571e0

QD
type: SiteQuality
SIO_000300: 1.429e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.246e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

VQSLOD
type: SiteQuality
SIO_000300: 7.3e-1

QD
type: SiteQuality
SIO_000300: 1.429e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.246e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

FS
type: SiteQuality
SIO_000300: 1.571e0

DP
type: SiteQuality
SIO_000300: 2.454817e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-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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bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.2e0

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

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQRankSum
type: SiteQuality
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FS
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66222
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73190162798753e-4
allele num: 11548
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8634
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

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

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

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

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
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allele num: 16498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Finnish)
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allele count: 2
allele frequency: 3.088326127239037e-4
allele num: 6476
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66220
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510117789187557e-5
allele num: 66220
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

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

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

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

East Asian
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allele count: 0
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allele num: 8636
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

VQSLOD
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DP
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66114
num of homozygotes: 0

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

African
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allele frequency: 1.96811651249754e-4
allele num: 10162
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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ClippingRankSum
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SIO_000300: 1.66e0

VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
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FS
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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QD
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SIO_000300: 1.32e1

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

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

South Asian
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allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66132
num of homozygotes: 0

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

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

FS
type: SiteQuality
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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SIO_000300: 1.081e1

MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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ClippingRankSum
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SIO_000300: -4.15e-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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.515472979116782e-5
allele num: 65986
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.384987e6

QD
type: SiteQuality
SIO_000300: 1.378e1

InbreedingCoeff
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SIO_000300: 1.7e-3

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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MQ
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ClippingRankSum
type: SiteQuality
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MQRankSum
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BaseQRankSum
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SIO_000300: -1.913e0

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-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: 1

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.237011380504701e-4
allele num: 8084
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2782
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4164
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21158
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

QD
type: SiteQuality
SIO_000300: 1.064e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.447e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.54773e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 6.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.81e-2

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.719207173194903e-5
allele num: 21190
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.58039e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.85e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 2.077e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.218e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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: 0
allele frequency: 0.0e0
allele num: 2860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1344
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1748
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4246
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South Asian
type: Population
allele count: 1
allele frequency: 1.218323586744639e-4
allele num: 8208
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.795e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

BaseQRankSum
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SIO_000300: -2.769e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.74e-2

VQSLOD
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ReadPosRankSum
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.66655e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
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)
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allele count: 1
allele frequency: 4.475875033569063e-5
allele num: 22342
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 6.08896e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.68e-2

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 2.233139794551139e-3
allele num: 4478
num of homozygotes: 0

Latino
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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allele num: 320
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East Asian
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South Asian
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FS
type: SiteQuality
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DP
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
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African
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allele frequency: 1.094238499330058e-2
allele num: 4478
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South Asian
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allele frequency: 2.354048964218456e-4
allele num: 8496
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Latino
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allele frequency: 1.63576881134133e-3
allele num: 1834
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Other
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allele frequency: 0.0e0
allele num: 320
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European (Non-Finnish)
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allele count: 8
allele frequency: 3.581341212284e-4
allele num: 22338
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 6.993006993006993e-4
allele num: 1430
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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QD
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MQ
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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MQRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 221
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.200768491834774e-4
allele num: 8328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21950
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1712
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.65e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.744e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 6.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.38549e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1694
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.506128334534967e-5
allele num: 22192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.59e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

DP
type: SiteQuality
SIO_000300: 6.44168e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.508e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
all individuals: 78
bin: 9.25e1
variant carriers: 0

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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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1996
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.296270836913559e-5
allele num: 23276
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.656e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.165e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.074e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

DP
type: SiteQuality
SIO_000300: 6.65413e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.36e-2

QD
type: SiteQuality
SIO_000300: 1.14e1

GenotypeQuality
all individuals: 128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8658
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.611672278338945e-4
allele num: 1782
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2076
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4730
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23722
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 6.7827e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.24e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

MQ
type: SiteQuality
SIO_000300: 5.192e1

QD
type: SiteQuality
SIO_000300: 5.41e0

GenotypeQuality
all individuals: 8778
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 250
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2933
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.46448087431694e-4
allele num: 1830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4804
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24360
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.904e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.367e0

MQRankSum
type: SiteQuality
SIO_000300: -2.367e0

MQ
type: SiteQuality
SIO_000300: 6.083e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.98992e5

QD
type: SiteQuality
SIO_000300: 6.1e0

GenotypeQuality
all individuals: 827
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8582
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 887
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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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variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.058771004139947e-5
allele num: 24638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1812
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2182
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8890
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.214e0

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

FS
type: SiteQuality
SIO_000300: 2.336e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.93e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

DP
type: SiteQuality
SIO_000300: 7.03371e5

VQSLOD
type: SiteQuality
SIO_000300: -1.208e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

QD
type: SiteQuality
SIO_000300: 5.64e0

GenotypeQuality
all individuals: 1062
bin: 1.25e1
variant carriers: 164

GenotypeQuality
all individuals: 813
bin: 4.75e1
variant carriers: 534

GenotypeQuality
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bin: 2.25e1
variant carriers: 426

GenotypeQuality
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bin: 6.75e1
variant carriers: 293

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 450

GenotypeQuality
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bin: 8.25e1
variant carriers: 661

GenotypeQuality
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bin: 2.75e1
variant carriers: 251

GenotypeQuality
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variant carriers: 10677

GenotypeQuality
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variant carriers: 558

GenotypeQuality
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variant carriers: 598

GenotypeQuality
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bin: 5.75e1
variant carriers: 222

GenotypeQuality
all individuals: 206
bin: 9.25e1
variant carriers: 158

GenotypeQuality
all individuals: 537
bin: 5.25e1
variant carriers: 280

South Asian
type: Population
allele count: 1729
allele frequency: 1.701101928374656e-1
allele num: 10164
num of homozygotes: 138

European (Finnish)
type: Population
allele count: 455
allele frequency: 2.183301343570058e-1
allele num: 2084
num of homozygotes: 21

Other
type: Population
allele count: 103
allele frequency: 2.31981981981982e-1
allele num: 444
num of homozygotes: 11

Latino
type: Population
allele count: 1953
allele frequency: 4.303657999118554e-1
allele num: 4538
num of homozygotes: 261

African
type: Population
allele count: 517
allele frequency: 9.762084592145015e-2
allele num: 5296
num of homozygotes: 18

European (Non-Finnish)
type: Population
allele count: 6488
allele frequency: 2.098182523769485e-1
allele num: 30922
num of homozygotes: 411

East Asian
type: Population
allele count: 4023
allele frequency: 6.96985446985447e-1
allele num: 5772
num of homozygotes: 1341

VQSLOD
type: SiteQuality
SIO_000300: 5.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.236e-1

QD
type: SiteQuality
SIO_000300: 1.68e1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

DP
type: SiteQuality
SIO_000300: 7.77395e5

GenotypeQuality
all individuals: 2881
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1066
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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: 92
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GenotypeQuality
all individuals: 1050
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5058
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.938065577623693e-5
allele num: 34036
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2334
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-3

QD
type: SiteQuality
SIO_000300: 1.33e1

MQ
type: SiteQuality
SIO_000300: 5.911e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.926e-1

FS
type: SiteQuality
SIO_000300: 9.585000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

DP
type: SiteQuality
SIO_000300: 8.02287e5

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

GenotypeQuality
all individuals: 946
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 826
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GenotypeQuality
all individuals: 339
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variant carriers: 2

GenotypeQuality
all individuals: 352
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GenotypeQuality
all individuals: 3675
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GenotypeQuality
all individuals: 1033
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GenotypeQuality
all individuals: 1111
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GenotypeQuality
all individuals: 4181
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GenotypeQuality
all individuals: 24913
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GenotypeQuality
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GenotypeQuality
all individuals: 2757
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GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 446
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variant carriers: 0

GenotypeQuality
all individuals: 1727
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.458217346214726e-5
allele num: 36642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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MQRankSum
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QD
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FS
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VQSLOD
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ClippingRankSum
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SIO_000300: 9.3e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

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

Latino
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allele frequency: 1.759324419422942e-4
allele num: 5684
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 2.602269178723847e-5
allele num: 38428
num of homozygotes: 0

Other
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
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FS
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MQRankSum
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VQSLOD
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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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South Asian
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Other
type: Population
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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: 7.468259895444362e-5
allele num: 40170
num of homozygotes: 0

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

African
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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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num of homozygotes: 0

VQSLOD
type: SiteQuality
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QD
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MQRankSum
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SIO_000300: 7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
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DP
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-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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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 542
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6152
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 2888
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)
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allele count: 1
allele frequency: 2.400384061449832e-5
allele num: 41660
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6770
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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VQSLOD
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MQRankSum
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BaseQRankSum
type: SiteQuality
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DP
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SIO_000300: 9.41011e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-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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East Asian
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allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.317926846228733e-5
allele num: 43142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3020
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11900
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.111e0

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.6704e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.079e-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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European (Non-Finnish)
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allele frequency: 2.243560979987436e-5
allele num: 44572
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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Other
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East Asian
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allele frequency: 1.509206157561123e-4
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European (Non-Finnish)
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South Asian
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Latino
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MQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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MQ
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FS
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ReadPosRankSum
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BaseQRankSum
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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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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Other
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Latino
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South Asian
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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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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African
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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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East Asian
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European (Non-Finnish)
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allele num: 46312
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Latino
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.35e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.019889e6

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.002e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.198e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6818
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.097843416967358e-5
allele num: 47668
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.043e1

VQSLOD
type: SiteQuality
SIO_000300: -1.57e0

MQRankSum
type: SiteQuality
SIO_000300: 6.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.88e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

MQ
type: SiteQuality
SIO_000300: 5.741e1

DP
type: SiteQuality
SIO_000300: 1.043531e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.248e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6924
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12712
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.048005242893422e-5
allele num: 48828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.33e0

DP
type: SiteQuality
SIO_000300: 1.062742e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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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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GenotypeQuality
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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
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49756
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7000
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.788161993769471e-5
allele num: 12840
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.189e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQ
type: SiteQuality
SIO_000300: 5.782e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.148e0

VQSLOD
type: SiteQuality
SIO_000300: -1.77e0

FS
type: SiteQuality
SIO_000300: 1.105e0

DP
type: SiteQuality
SIO_000300: 1.079455e6

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

QD
type: SiteQuality
SIO_000300: 1.033e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7094
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8064
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.731067847528384e-4
allele num: 51262
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.62e0

FS
type: SiteQuality
SIO_000300: 2.435e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

DP
type: SiteQuality
SIO_000300: 1.099614e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.811250581125058e-5
allele num: 51624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8138
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13140
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.260398285858331e-4
allele num: 7934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 656
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3806
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.94e-1

FS
type: SiteQuality
SIO_000300: 7.2e-1

QD
type: SiteQuality
SIO_000300: 1.098e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 1.104536e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.94e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7980
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3946
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
type: Population
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allele frequency: 7.500750075007501e-5
allele num: 13332
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.115246e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.103e0

QD
type: SiteQuality
SIO_000300: 7.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 7.432733759476735e-5
allele num: 13454
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52258
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Other
type: Population
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7962
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3980
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.502e0

DP
type: SiteQuality
SIO_000300: 1.08819e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.59e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 1.3704e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 335
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variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3990
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52226
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.429420505200594e-5
allele num: 13460
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Other
type: Population
allele count: 0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
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allele num: 7018
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -6.632e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.227e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13388
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6916
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.224289911851126e-4
allele num: 8168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3922
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.066985e6

FS
type: SiteQuality
SIO_000300: 6.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.067e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.6e0

VQSLOD
type: SiteQuality
SIO_000300: -2.377e0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 5.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

MQ
type: SiteQuality
SIO_000300: 5.728e1

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: 9

GenotypeQuality
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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: 88
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.564027370478983e-4
allele num: 51150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3882
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.446016381236039e-5
allele num: 13430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8088
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.66e-1

QD
type: SiteQuality
SIO_000300: 1.286e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.309e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.045989e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 29

GenotypeQuality
all individuals: 409
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GenotypeQuality
all individuals: 192
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variant carriers: 1

African
type: Population
allele count: 30
allele frequency: 3.846153846153846e-3
allele num: 7800
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.484472049689441e-4
allele num: 8050
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3866
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.148e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.344e0

DP
type: SiteQuality
SIO_000300: 1.037597e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.43e0

QD
type: SiteQuality
SIO_000300: 1.243e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-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
all individuals: 1130
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.280737704918033e-4
allele num: 7808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8032
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3896
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.964559349337943e-5
allele num: 50902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6788
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.075e0

QD
type: SiteQuality
SIO_000300: 6.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

DP
type: SiteQuality
SIO_000300: 1.032231e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.611e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

GenotypeQuality
all individuals: 188
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variant carriers: 0

GenotypeQuality
all individuals: 2277
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3290
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7808
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3896
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.473187978786093e-4
allele num: 6788
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50902
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

FS
type: SiteQuality
SIO_000300: 7.611e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

DP
type: SiteQuality
SIO_000300: 1.032231e6

QD
type: SiteQuality
SIO_000300: 6.87e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.9e-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
all individuals: 1078
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GenotypeQuality
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GenotypeQuality
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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: 28

GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 1991
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3842
num of homozygotes: 0

African
type: Population
allele count: 27
allele frequency: 3.4856700232378e-3
allele num: 7746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.988783262400064e-5
allele num: 50282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13402
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.256913021618904e-4
allele num: 7956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 646
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.362e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

DP
type: SiteQuality
SIO_000300: 1.015721e6

QD
type: SiteQuality
SIO_000300: 2.697e1

MQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1908
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13370
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.297690111601349e-4
allele num: 7706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50070
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3826
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.129e0

QD
type: SiteQuality
SIO_000300: 6.21e0

DP
type: SiteQuality
SIO_000300: 1.008346e6

MQRankSum
type: SiteQuality
SIO_000300: 7.85e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.126e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.013e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1978
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GenotypeQuality
all individuals: 690
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GenotypeQuality
all individuals: 870
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GenotypeQuality
all individuals: 21790
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 468
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GenotypeQuality
all individuals: 479
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50016
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3822
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7854
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.495128166691651e-5
allele num: 13342
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.005213e6

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.51e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

FS
type: SiteQuality
SIO_000300: 2.834e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.7e-1

QD
type: SiteQuality
SIO_000300: 2.94e1

GenotypeQuality
all individuals: 97
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 343
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 4011
bin: 2.75e1
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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
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3726
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.547169811320755e-5
allele num: 13250
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 9.283819628647215e-4
allele num: 7540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.04398659144796e-5
allele num: 48924
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.593360995850622e-4
allele num: 7712
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -7.677e-1

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.96e-1

MQRankSum
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QD
type: SiteQuality
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FS
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ClippingRankSum
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SIO_000300: -5.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-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

African
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allele frequency: 0.0e0
allele num: 7386
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.516530178950561e-4
allele num: 13188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3610
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.303101381287464e-4
allele num: 7674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
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allele frequency: 0.0e0
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.48e-1

ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 5.8e-2

InbreedingCoeff
type: SiteQuality
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DP
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FS
type: SiteQuality
SIO_000300: 1.392e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 6262
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 9.528995371630819e-4
allele num: 7346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.158522892668524e-5
allele num: 48094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13130
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 9.61e-1

QD
type: SiteQuality
SIO_000300: 1.319e1

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

DP
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SIO_000300: 9.51101e5

VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.763957987838585e-4
allele num: 7236
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47286
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.658140603461479e-5
allele num: 13058
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

DP
type: SiteQuality
SIO_000300: 9.31739e5

BaseQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

QD
type: SiteQuality
SIO_000300: 1.041e1

FS
type: SiteQuality
SIO_000300: 1.849e0

VQSLOD
type: SiteQuality
SIO_000300: 3.92e-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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

FS
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.028e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -6.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.659e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 5.14e0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.200123206899586e-5
allele num: 45452
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Latino
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African
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
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FS
type: SiteQuality
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VQSLOD
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DP
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SIO_000300: 8.80391e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

Other
type: Population
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allele num: 578
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South Asian
type: Population
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allele frequency: 1.576044129235619e-4
allele num: 12690
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 6.724949562878279e-5
allele num: 44610
num of homozygotes: 0

MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
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QD
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DP
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InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -2.32e-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

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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African
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Other
type: Population
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allele frequency: 0.0e0
allele num: 574
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.239441035517535e-5
allele num: 44654
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East Asian
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South Asian
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BaseQRankSum
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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VQSLOD
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ClippingRankSum
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QD
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DP
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2440
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3088
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.908889591901297e-5
allele num: 12644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6778
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44364
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.407e0

QD
type: SiteQuality
SIO_000300: 5.32e0

VQSLOD
type: SiteQuality
SIO_000300: -1.997e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.481e0

MQRankSum
type: SiteQuality
SIO_000300: -9.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

DP
type: SiteQuality
SIO_000300: 8.64312e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 5.756e1

GenotypeQuality
all individuals: 2456
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11493
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4897
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2583
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 194
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6994
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3070
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.751313485113835e-4
allele num: 5710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6714
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

DP
type: SiteQuality
SIO_000300: 8.58247e5

FS
type: SiteQuality
SIO_000300: 1.583e0

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.868e0

QD
type: SiteQuality
SIO_000300: 3.15e0

GenotypeQuality
all individuals: 2331
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4840
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2699
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 25764
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 255
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1038
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11861
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 94
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 9
allele frequency: 7.2e-4
allele num: 12500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.835957222196723e-4
allele num: 43574
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.484320557491289e-3
allele num: 574
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 5.366726296958855e-4
allele num: 5590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3000
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6900
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.81e-1

DP
type: SiteQuality
SIO_000300: 8.51124e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.212e1

GenotypeQuality
all individuals: 2229
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 103
bin: 8.75e1
variant carriers: 10

GenotypeQuality
all individuals: 700
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1302
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 782
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 655
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 279
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 429
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 200
bin: 8.25e1
variant carriers: 11

GenotypeQuality
all individuals: 2702
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4974
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1045
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 687
bin: 9.75e1
variant carriers: 371

GenotypeQuality
all individuals: 1225
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 11946
bin: 6.25e1
variant carriers: 6

GenotypeQuality
all individuals: 367
bin: 7.25e1
variant carriers: 4

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2978
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.52112676056338e-3
allele num: 568
num of homozygotes: 0

African
type: Population
allele count: 391
allele frequency: 5.917070217917676e-2
allele num: 6608
num of homozygotes: 10

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 2.078233962961252e-4
allele num: 43306
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.028259473346178e-5
allele num: 12456
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 2.198768689533861e-3
allele num: 6822
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.60100828231905e-4
allele num: 5554
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

DP
type: SiteQuality
SIO_000300: 8.50218e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 5.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 1.299e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

GenotypeQuality
all individuals: 1245
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26540
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5095
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2712
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 194
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2208
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.306060326538142e-5
allele num: 43364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2970
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6862
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.41815e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.69e0

FS
type: SiteQuality
SIO_000300: 1.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 6.047e1

QD
type: SiteQuality
SIO_000300: 1.413e1

GenotypeQuality
all individuals: 988
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2826
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5172
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26390
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4876
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 673
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.327855114297686e-5
allele num: 42958
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2946
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.34359e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

MQ
type: SiteQuality
SIO_000300: 5.906e1

FS
type: SiteQuality
SIO_000300: 8.022e0

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.936e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 5.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.426e0

GenotypeQuality
all individuals: 598
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 11422
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26746
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4925
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5202
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.343237416815072e-5
allele num: 42676
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6314
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6744
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.282e-1

FS
type: SiteQuality
SIO_000300: 2.105e0

QD
type: SiteQuality
SIO_000300: 1.751e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

DP
type: SiteQuality
SIO_000300: 8.28091e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 587
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 196
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 96
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 203
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27004
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2972
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 5293
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1000
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2196
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4989
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1253
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 351
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 4.465614766299494e-4
allele num: 6718
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2894
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.601024655779699e-4
allele num: 6246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 30
allele frequency: 7.076139258420605e-4
allele num: 42396
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5390
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

QD
type: SiteQuality
SIO_000300: 1.36e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.66e0

FS
type: SiteQuality
SIO_000300: 1.741e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

DP
type: SiteQuality
SIO_000300: 8.19832e5

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1